A Revies of: Some Truth with Maps; A Primer on Symbolisation & Design.

In this article, we present a geographically explicit agent-based model (ABM), loosely coupled with vector geographical information systems (GISs), which explicitly captures and uses geometric data and socioeconomic attributes in the simulation process. The ability to represent the urban environment as a series of points, lines, and polygons not only allows one to represent a range of different-sized features such as buildings or larger areas portrayed as the urban environment but is a move away from many ABMs utilizing GIS that are rooted in grid-based structures. We apply this model to the study of residential segregation, specifically creating a Schelling (1971 Schelling, T.C. 1971. Dynamic models of segregation. Journal of Mathematical Sociology, 1(1): 143–186. [Taylor &; Francis Online] , [Google Scholar]) type of model within a hypothetical cityscape, thus demonstrating how this approach can be used for linking vector-based GIS and agent-based modeling. A selection of simulation experiments are presented, highlighting the inner workings of the model and how aggregate patterns of segregation can emerge from the mild tastes and preferences of individual agents interacting locally over time. Furthermore, the article suggests how this model could be extended and demonstrates the importance of explicit geographical space in the modeling process.     

Climate change in lowland Central America during the late deglacial and early Holocene

The transition from arid glacial to moist early Holocene conditions represented a profound change in northern lowland Neotropical climate. Here we report a detailed record of changes in moisture availability during the latter part of this transition (～11 250 to 7500 cal. yr BP) inferred from sediment cores retrieved in Lake Petén Itzá, northern Guatemala. Pollen assemblages demonstrate that a mesic forest had been largely established by ～11 250 cal. yr BP, but sediment properties indicate that lake level was more than 35 m below modern stage. From 11 250 to 10 350 cal. yr BP, during the Preboreal period, lithologic changes in sediments from deep‐water cores (>50 m below modern water level) indicate several wet–dry cycles that suggest distinct changes in effective moisture. Four dry events (designated PBE1‐4) occurred centred at 11 200, 10 900, 10 700 and 10 400 cal. yr BP and correlate with similar variability observed in the Cariaco Basin titanium record and glacial meltwater pulses into the Gulf of Mexico. After 10 350 cal. yr BP, multiple sediment proxies suggest a shift to a more persistently moist early Holocene climate. Comparison of results from Lake Petén Itzá with other records from the circum‐Caribbean demonstrates a coherent climate response during the entire span of our record. Furthermore, lowland Neotropical climate during the late deglacial and early Holocene period appears to be tightly linked to climate change in the high‐latitude North Atlantic. We speculate that the observed changes in lowland Neotropical precipitation were related to the intensity of the annual cycle and associated displacements in the mean latitudinal position of the Intertropical Convergence Zone and Azores–Bermuda high‐pressure system. This mechanism operated on millennial‐to‐submillennial timescales and may have responded to changes in solar radiation, glacial meltwater, North Atlantic sea ice, and the Atlantic meridional overturning circulation (MOC). Copyright © 2005 John Wiley & Sons, Ltd.     

Future trends in transport and fate of diffuse contaminants in catchments,with special emphasis on stable isotope applications

A summary is provided of the first of a series of proposed Integrated Science Initiative workshops supported by the UNESCO International Hydrological Programme. The workshop brought together hydrologists, environmental chemists, microbiologists, stable isotope specialists and natural resource managers with the purpose of communicating new ideas on ways to assess microbial degradation processes and reactive transport at catchment scales. The focus was on diffuse contamination at catchment scales and the application of compound‐specific isotope analysis (CSIA) in the assessment of biological degradation processes of agrochemicals. Major outcomes were identifying the linkage between water residence time distribution and rates of contaminant degradation, identifying the need for better information on compound specific microbial degradation isotope fractionation factors and the potential of CSIA in identifying key degradative processes. In the natural resource management context, a framework was developed where CSIA techniques were identified as practically unique in their capacity to serve as distributed integrating indicators of process across a range of scales (micro to diffuse) of relevance to the problem of diffuse pollution assessment. Copyright © 2006 John Wiley & Sons, Ltd.     

The Relative Lyapunov Indicator: An Efficient Method of Chaos Detection

A recently introduced chaos detection method, the relative Lyapunov indicator (RLI) is investigated in the cases of symplectic mappings and of a continuous Hamiltonian system. It is shown that the RLI is an efficient and easy-to-calculate numerical tool in determining the true nature of individual orbits, and in separating ordered and regular regions of the phase space of dynamical systems. An application of the RLI for stability investigations of some recently discovered exoplanetary systems is also presented.     

Mercury mobility and bioavailability in soil from contaminated area

The mobility and bioavailability of mercury in the soil from the area near a plant using elemental mercury for manufacturing thermometers, areometers, glass energy switches and other articles made of technical glass has been evaluated. Mercury has been determined by sequential extraction method and with additional thermo desorption stage to determine elemental mercury. The procedure of sequential extraction involves five subsequent stages performed with the solutions of chloroform, deionized water, 0.5 M HCl, 0.2 M NaOH and aqua regia. The mean concentration of total mercury in soil was 147 ± 107 μg g⁻¹ dry mass (range 62–393), and the fractionation revealed that mercury was mainly bound to sulfides 56 ± 8% (range 45–66), one of the most biounavailable and immobile species of mercury in the environment. The fractions that brought lower contribution to the total mercury content were semi-mobile humic matter 22 ± 9% (range 11–34) and elemental mercury 17 ± 5% (range 8–23). The contributions brought by the highly mobile and toxic organomercury compounds were still lower 2.3 ± 2.7% (range 0.01–6.5). The lowest contributions brought the acid-soluble mercury 1.5 ± 1.3% (range 0.1–3.5) and water-soluble mercury 1.0 ± 0.3% (range 0.6–1.7). The surface layer of soil (0–20 cm) was characterized by higher mercury concentrations than that of the subsurface soil (60–80 cm), but the fractional contributions were comparable. The comparison of mercury fractionation results obtained in this study for highly polluted soils with results of fractionation of uncontaminated or moderately contaminated samples of soil and sediments had not shown significant statistical differences; however, in the last samples elemental mercury is usually present at very low concentrations. On the basis of obtained correlation coefficients it seems that elemental mercury soils from “Areometer” plant are contaminated; the main transformation is its vaporization to atmosphere and oxidation to divalent mercury, probably mainly mediated by organic matter, and next bound to humic matter and sulfides.     

Direct versus indirect determination of suspended sediment associated metals in a mining-influenced watershed

The differentiation between the concentration of metals associated with suspended sediments and those in the dissolved phase is often of importance in aquatic ecosystems, for such reasons as toxicity evaluation, total maximum daily load calculations, and a better understanding of metal transport. Often, published water quality data include only concentrations of total and dissolved metals, with particulate concentrations assumed equal to the difference between the two. The validity of this assumption for mining-influenced waters is addressed in this paper by comparing data determined from the subtraction of total (acid-soluble) and dissolved (operationally defined as less than 0.45-μm) metal concentrations (difference method) with data obtained from acid-digestion of the particles retained on the filters used for filtering the dissolved fraction (digestion method). Greater than fifty water samples containing suspended sediment were collected from each of three sites in the Clear Creek Watershed in Colorado during a two and one-half year study on the fate and transport of metals in the watershed. Volumes of water filtered ranged from 50 to 250 ml, representative of typical volumes used for the determination of dissolved metal concentrations. The particulate-associated concentrations of Al, Cu, Fe, Mn, and Zn determined from the difference method compared well with the concentrations determined by the digestion method. Statistical analyses indicated that there is not a statistically significant difference between the two methods at the 95% confidence level, with p-values of 0.65, 0.88, 0.39, 0.67, and 0.75, for Al, Cu, Fe, Mn, and Zn, respectively, over the three sites.