A case study of social behaviour in a natural disaster: the olivares landslide (Spain)

The modern sociological literature on disasters highlights the fact that many of the ideas about human behaviour in disasters which were long considered as valid, are wrong. The main discovery is based on the fact that situations of crisis increase people's moral principles and capability of response. This paper illustrates some of these ideas, in a case study of a village which was struck by a natural disaster in the north of Granada (Spain) in 1986. The population's attitude revealed a huge potential of resources that were underestimated by professionals of disaster management. The analysis shows that it is necessary to bring civil protection systems and the population's capability of response into close harmony.     

Variation in some chemical parameters and organic matter in soils regenerated by the addition of municipal solid waste

The organic fraction of a municipal solid waste was added in different doses to an eroded soil formed of loam and with no vegetal cover. After three years, the changes in macronutrient content and the chemical-structural composition of its organic matter were studied. The addition of the organic fraction from a municipal solid waste had a positive effect on soil regeneration, the treated soils being covered with spontaneous vegetation from 1 yr onwards. An increase in electrical conductivity and a fall in pH were noted in the treated soils as were increases in macronutrients, particularly N and available P and the different carbon fractions. Optical density measurements of the organic matter extracted with sodium pyrophosphate showed that the treated soils contained an organic matter with less condensed compounds and with a greater tendency to evolve than the control. A pyrolysis-gas chromatography study of the organic matter extracted with pyrophosphate showed large quantities of benzene both in the treated soils and control; pyrrole was also relatively abundant, although this fragment decreased as the dose rose. Xylenes and pyridine were present in greater quantities in the control and furfural in the treated soils. Three years after addition to the soil, the organic matter had a higher proportion of fragments derived from aromatic compounds and a smaller proportion derived from hydrocarbons. Similarity indices showed that, although the added and newly formed organic matter 3 yr after addition continued to differ from that of the original soil and to be more mineralizable, the transformations it has undergone made it more similar to the original organic matter of the soil than it was at the moment of being added.     

Comparison between chemical and isotopic measurements of biological nitrate utilization: further evidence of low new-production levels in the equatorial Pacific

New-production (nitrate uptake) rates in the equatorial Pacific were estimated by parallel measurements of nitrate disappearance from sea water using a colorimetric method and of ¹⁵N-labelled nitrate (¹⁵NO₃ ⁻) incorporation into particulate organic nitrogen (PON) collected on GF/F filters (net nitrate uptake, conventional ¹⁵N-tracer method) and Anopore (0.2 μm) membranes. Regression analyses of 74 sample pairs gathered during 12 and 24 h productivity experiments revealed a significant positive relationship between decreasing nitrate level and ¹⁵NO₃ ⁻ accumulation into PON retained on GF/F filters, but the slopes of Model I and Model II regression lines were 1.18 and 1.29, respectively, suggesting that 15 to 22% of ¹⁵NO₃ ⁻ removed from the dissolved fraction were lost to another N-pool. Two possible avenues for the missing ¹⁵NO₃ ⁻ have been examined: uptake by submicron particles passed through the GF/F filters, and loss as dissolved organic nitrogen (DON). Nitrate uptake by small cells not recovered on GF/F filters, could be safely eliminated as a cause of loss, since ¹⁵NO₃ ⁻ uptake rates obtained from ¹⁵N entering PON collected on GF/F filters agreed well with those obtained from ¹⁵N entering PON collected on Anopore membranes (32 sample pairs). Inspection of the DON pool of 0.2 μm filtrates for excess-¹⁵N enrichment (20 samples) revealed that in nitrate-rich waters (equatorial upwelling between 1°N and 10°S), loss of ¹⁵NO₃ ⁻ as DO¹⁵N accounted for <5% of net nitrate uptake. In samples from subtropical oligotrophic waters (from 11°S southward), however, ¹⁵NO₃ loss as DO¹⁵N represented up to 20% of net NO₃ ⁻ uptake. These results, as well as experimental considerations concerning the use of colorimetric and isotopic methods to measure new production show that: (1) earlier reported high discrepancies between nitrate decreases (ΔNO₃ ⁻) and ¹⁵NO₃ ⁻ incorporation into filterable particles (ΔNO₃ ⁻/¹⁵NO₃ ⁻ incorporation >2) were probably erroneous; (2) the use of GF/F filters does not result in an underestimation of new production, although it was found to underestimate PON concentrations by up to 60%; (3) in the equatorial upwelling area (1°N to 10°S), which has high ambient nitrate levels (>2000 nmol l⁻¹) but only slight changes in concentration (0 to 80 nmol l⁻¹ d⁻¹), new production is more accurately estimated by the isotopic method than by the chemical method; (4) in subtropical oligotrophic waters (from 11°S southward) with low ambient nitrate levels (0 to 100 nmol l⁻¹), both procedures are appropriate as long as nitrate removal per incubation period is >3 nmol l⁻¹ (lower rates are only detectable with the isotopic method); (5) the traditional ¹⁵N-tracer technique does not substantially underestimate net new-production in the equatorial Pacific, and failure to account for the loss of ¹⁵NO₃ ⁻ as DON, i.e. to estimate gross nitrate uptake (gross uptake = net uptake + ¹⁵N loss) tends to underestimate new production on an average by only 10%. Overall, the apparent low level of new production in the nitrate-rich area of the central equatorial Pacific seems to be a fact, and may be ascribable to other nutrient (macro and micro) deficiencies and/or to intense in situ recycling of ammonium and nitrate (regenerated production) rather than to inaccurate nitrate uptake rates measured with the classical ¹⁵N-tracer technique. Received: 24 November 1998 / Accepted 10 March 2000     

Carbon and nitrogen exchange between sandy beach clams (Donax serra) and kelp beds in the Benguela coastal upwelling region

Carbon consumption and nitrogen requirements were estimated for populations of the sandy beach bivalve Donax serra on nine beaches of the west coast of South Africa. Subtidal populations composed mainly of adult clams were responsible for the bulk of standing stock (3538 g C m⁻¹), annual carbon consumption (13 444 g C m⁻¹ yr⁻¹), faeces production (6478 g C m⁻¹ yr⁻¹ ) and nitrogen regeneration (2525 g N m⁻¹ yr⁻¹). Kelp detritus, bacteria and kelp consumers' faeces available in the water column surpass several times the carbon and nitrogen requirements of intertidal and subtidal clam populations. Individual Donax serra pop ulations, in turn, may regenerate up to 3.2% of the total nitrogen requirements of all primary producers from kelp beds and 14% of the requirements of phytoplankton. These high standing stocks of clams are presumably supported mainly by organic matter originating from kelp which, in contrast to phytoplankton, is in constant supply and comprises the largest proportion of the annual production of particulate organic matter on this coast. Wide and shallow continental shelves with gentle slopes probably limit the penetration of upwelled waters to the nearshore waters, decreasing the influence of external inputs and increasing the importance of internal flows of nutrients and carbon within the nearshore zone. In this context, sandy beaches, rocky shores and kelp beds may be more closely interlinked compartments of a larger ecosystem encompassing the whole nearshore than traditionally thought. Received: 28 August 1996 / Accepted: 7 October 1996     

Trace gases and particulate matter emissions from wildfires and agricultural burning in Northeastern Mexico during the 2000 fire season

An inventory of air pollutants emitted from forest and agricultural fires in Northeastern Mexico for the period of January to August of 2000 is presented. The emissions estimates were calculated using an emissions factor methodology. The inventory accounts for the emission of carbon monoxide (CO), methane, nonmethane hydrocarbons, ammonia, nitrogen oxides, and particulate matter (PM). Particulate matter emissions include estimates for fine PM and coarse PM. A total of 2479 wildfires were identified in the domain for the period of interest, which represented approximately 810,000 acres burned and 621,130 short tons emitted (81% being CO). The main source of information used to locate and estimate the extent of the fires came from satellite imagery. A geographic information system was used to determine the type of vegetation burned by each fire. More than 54% of the total area burned during the period of study was land on the State of Tamaulipas. However, >58% of the estimated emissions came from the State of Coahuila. This was because of the mix of vegetation types burned in each state. With respect to the temporal distribution, 76.9% of the fires occurred during the months of April and May consuming almost 78% of the total area burned during the period of study. Analysis of wind forward trajectories of air masses passing through the burned areas and 850-mb wind reanalyses indicate possible transboundary transport of the emissions from Mexico to the United States during the occurrence of the major wildfires identified.     

Evaluation of heavy metal availability in polluted soils by two sequential extraction procedures using factor analysis

Superficial soil and grass samples from 13 locations affected by several anthropogenic sources (mining, metal factory, traffic emissions) were collected in Gipuzkoa, northern Spain. The more labile metal fractions, the mobile (extracted by 0.01 mol l(-1) CaCl(2)) and the mobilisable (extracted by 0.005 mol l(-1) DTPA), were evaluated using a short sequential procedure with two steps. From the results a short-medium term potential lability of Cd, Cu, Zn and Pb can be concluded. The labile levels were compared with the results obtained using the Tessier sequential procedure. Factor analysis was used to check the associations between the total metal contents in soil and grass, as well as between the levels of the different sequential fractions and the total content in grass. Cd, Cu and Zn labile levels were related to total metal grass contents indicating its suitability for the availability studies in polluted soil-plant system.     

In vivo evaluation of three biomarkers in the mosquitofish (Gambusia yucatana) exposed to pesticides

In this study, the acute toxicity and the in vivo effects of commercial chlorpyrifos, carbofuran and glyphosate formulations on cholinesterase (ChE), glutathione S-transferase (GST) and lactate dehydrogenase (LDH) activities of the mosquitofish (Gambusia yucatana) were investigated. In a first phase of the study, head and muscle ChE were characterized with different substrates (acetylthiocholine iodide, s-butyrylthiocholine iodide and propionylthiocholine iodide) and the selective inhibitors eserine hemisulfate, 1,5-bis(4-allyldimethylammoniumphenyl)-pentan-3-one dibromide (BW284C51), and N,N'-diisopropylphosphorodiamic acid (iso-OMPA). The results obtained suggest that the enzyme present in both head and muscle of G. yucatana is mainly acetylcholinesterase (AChE). Acute toxicity was evaluated by exposing fish to several concentrations of single pesticides and of a mixture of chlorpyrifos/glyphosate. LC50 values were determined after 96 h of exposure, except in the case of carbofuran for which LC50 was calculated after 24 h since almost all the fish died within this period. LC50 values were 0.085 mg/l for chlorpyrifos, 17.79 mg/l for glyphosate, 0.636 mg/l for carbofuran and 0.011 mg/l for the chlorpyrifos/glyphosate mixture. A Toxic Unit approach was used to compare the toxicity of chlorpyrifos and glyphosate when occurring in a mixture with their toxicities as single compounds. Synergistic effects of chlorpyrifos and glyphosate when present in a mixture were found. At the end of each bioassay (24 h for carbofuran, 96 for the other substances/mixture), effects on biomarkers were analyzed. Muscle LDH activity was not altered by any of the three pesticides tested. Gill GST activity was significantly inhibited (40%) by carbofuran after 24 h of exposure to concentrations equal or higher than 0.06 mg/l. ChE muscle and head activity were significantly inhibited (50% and 30%, respectively) by carbofuran at concentrations equal or higher than 0.25 mg/l. Chlorpyrifos induced a significant inhibition of both muscle and head ChE (80% and 50%, respectively) after 96 h of exposure to concentrations equal or higher than 0.05 mg/l. Carbofuran did not induce significant alterations of fish ChE. The ChE EC50 determined for chlorpyrifos/glyphosate mixture (0.070 mg/l) was higher than the correspondent value calculated for chlorpyrifos alone (0.011 mg/l) suggesting an antagonistic effect of glyphosate on ChE inhibition by chlorpyrifos. ChE activity of G. yucatana seems to be a good biomarker to diagnose the exposure of wild populations of this species exposed to anticholinesterase pesticides.     

Structure-activity relationships for association of linear alkylbenzene sulfonates with activated sludge

Sorption of linear alkylbenzene sulfonates (LAS) on sludge particles from wastewater treatment plants was studied. The effect of alkyl chain length and the water hardness were investigated. Sorption on sludge increases with increasing alkyl chain length in the LAS molecules. The results are interpreted in terms of a hydrophobic bonding mechanism being the critical micelle concentration a good index of the surfactant hydrophobicity. The increase in free energy of adsorption for the addition of successive methylene groups to the alkyl chain was estimated as 2.4 kJ/mol. Water hardness clearly enhances the sorption of LAS homologues on sludge and seems to promote cooperative sorption at high surfactant and calcium ion concentrations. An empirical equation was provided that allow to estimate the partition coefficient between aqueous and solid phases for LAS homologues as a function of the alkyl chain length and the water hardness.     

Sediments as monitors of heavy metal contamination in the Ave river basin (Portugal): multivariate analysis of data

The concentrations of heavy metals (Cd, Cr, Cu, Ni, Pb, Zn) were determined in river sediments collected at the Ave river basin (Portugal) to obtain a general classification scenery of the pollution in this highly polluted region. Multivariate data analysis techniques of clustering, principal components and eigenvector projections were used in this classification. Five general areas with different polluting characteristics were detected and several individual heavy metal concentration abnormalities were detected in restricted areas. A good correlation between the overall metal contamination determined by multivariate analysis and metal pollution indexes for all sampling stations was obtained. Some preliminary experiments showed that the metal concentrations normalised to the volatile matter content in the sediment fraction with grain size <63 microm seems to be an adequate method for assessing metal pollution.