Transfer of fishing effort between areas and fishery units in Spanish fisheries as side effects of the prestige oil spill management measures

This paper shows how post-oil spill management measures can affect the general pattern of fishing effort exerted on two particular species of great commercial value in northern Spanish fisheries: anglerfish (Lophius piscatorius and Lophius budegassa) and mackerel (Scomber scombrus). Data time series of catches and fishing efforts were analysed corresponding to the area and time period affected by the oil spill fishing restrictions (December 2002–June 2003) and similar previous and post-spill periods. This was done to detect shifts that could be due to either the oil spill per se or the management measures taken to minimise pollution effects. Then, analyses and simulations with Arcview GIS module FAST (Fishing Activity Simulation Tool v. 1.1) were carried out with the aim of studying the fishing effort spatial distribution. Changes were observed in the Catch Per Unit Effort (CPUE) of anglerfish and mackerel by area or fishery unit. Results show a spatial displacement of fishing effort to other fishing areas in the case of anglerfish, and the transfer of fishing effort between different fishery units in the case of mackerel. Although both effects were caused primarily by the management measures in force after the oil spill, they are considered side or collateral effects. The management measures that have to be taken after any disaster should also consider these kinds of ancillary effects as well as evaluating the likely positive or negative impact of these side effects.     

Re‐establishment of soil water repellency after destruction by intense burning in a Mediterranean heathland (SW Spain)

Soil water repellency has been conventionally considered as a fire‐induced effect, but an increasing number of studies have suggested that natural background repellency occurs in many soil types, and many of them have suggested that water repellency can be re‐established over time after being destroyed. An experimental fire was conducted to study changes of the soil surface during the first 18 months following intense burning. The main objectives of this paper are as follows: (1) to investigate in situ water repellency changes at three soil depths (0, 2 and 4 cm) immediately after burning; (2) to evaluate the medium‐term evolution of water repellency under field conditions; and (3) to outline the main hydrological consequences of these changes. Also, different water repellency tests (water drop penetration time, ethanol percentage test (EPT) and contact angle (CA) between water drops and the soil surface) were carried out for comparison purposes. Field experiments showed that soil water repellency was partly destroyed after intense burning. Changes were relatively strong at the soil surface, but diminished progressively with depth. Levels of water repellency were practically re‐established 18 months after burning. This suggests that water repellency in the studied area is not necessarily a consequence of fire, but can instead be a natural attribute. Finally, although limited in time, destruction of soil water repellency has important consequences for runoff flow generation and soil loss rates, and, indirectly, for water quality. Copyright © 2009 John Wiley & Sons, Ltd.     

Quantum mechanical potential surfaces and calculations on minerals and molecular clusters

Recently, ab-initio quantum mechanical potential surfaces calculated for silicate hydroxyacid molecules were used to extract covalent potentials for use in mineral physics calculations (Lasaga and Gibbs 1987). The calculations showed that these potentials are capable of generating the structure and physical properties of silicate minerals. In this paper we explore in more detail the suitability of various covalent potentials in mimicking the topography of the ab-initio potential surfaces. We also extend the use of such quantum-derived potentials in generating the structures of hydroxyacid dimers, trimers, and pentamers of silicate tetrahedra and in studying the structure and the dynamical properties of minerals and glasses.     

The objective determination of the instantaneous predominant frequency of seismic signals and inferences onQ of coda waves

A technique to detect spectrum variations versus time along seismic signals is applied to coda waves of local earthquakes (Friuli, Northern Italy). The technique consists of an autoregressive modeling and utilizes nonlinear spectral analysis where the spectrum of stochastic processes is estimated as the transfer function of the filter that whitens the process under analysis. This approach appears to be particularly well suited to those investigations where automatic measurements of the instantaneous frequency have to be carried out on digital data. The detection of variations of the instantaneous frequency along the coda allows computation of seismic-Q in the lithosphere and its frequency dependence: the result obtained is $$Q = 100f^{0.4} $$ which appears to be strongly consistent with that, based on the estimate of the coda amplitude decay in the band including the most significant frequencies of the signals under analysis.     

Association of subsurface radon changes in Alaska and the northeastern United States with earthquakes

Changes of radon concentration in the ground have been reported to correlate with seismic activity in many places over widely varying distances from the earthquake epicenters, sometimes over 100's and occasionally over 1000's of km depending on the magnitude M of the earthquakes. For proper use of such correlations in forecasting the location and size of impending earthquakes, it would be useful to establish a relation between M and the maximum distance x_M at which radon can be significantly altered by preseismic effects.We have monitored radon in the ground continuously at Blue Mountain Lake, NY starting Dec. 3. 1975 and at three locations in Alaska—Icy Bay, Yakataga, and Sand Point (starting Nov. 12, 1979; March 5, 1980; and June 29, 1980 respectively). Sample correlations from visual examination of the recent radon record and tentative use of a proposed scaling relation show a number of possible earthquake-related signals at these locations. The data are compatible with scaling relations that were derived from two separate models of premonitory elastic strains. In this work x_M = 10^0.48M, where x_M is in units of km and M ≥ 3. Since tilt and strain signals correlate similarly with magnitude and distance, it is likely that most earthquake-related radon signals are mechanically induced.     

Seismic Q for the lithosphere of the Montenegro region (Yugoslavia): frequency,depth and time windowing effects

The availability of accelerometric data for the Montenegro earthquake of 15th April 1979 makes it possible to investigate seismic Q of the lithosphere in that region, in particular, its dependence on frequency, on the depth reached by seismic waves, and on the length of time windows in which signals are processed. Two different spectral methods, S phase energy ratio and coda envelope decay, are applied, respectively, to direct and scattered shear waves. Similar results are obtained using different portions of the recordings, i.e., coda waves for the envelope decay fit and the S wave train, with a significant duration of ～ 10 s, for the energy ratios. The same apparent Q (Q ～ 40 f, where f is the frequency expressed in Hz) that is found for other neighbouring central Mediterranean regions (e.g., Ancona, on the central Italian Adriatic coast; Valnerina, in the central Apennines; Irpinia, in the southern Apennines) is also found for the southern Yugoslavian coast, in the band 1–25 Hz up to a maximum range of ～ 120 km from the focus. This strong frequency dependence is probably connected with the type of small-scale heterogeneity and the same geological age and level of tectonic activity peculiar to all these seismotectonic areas.In order to compare the apparent Q of the whole S wave train, ～ 10 s long, with the (intrinsic) apparent Q of the single direct S wave (usually 1 s or less), the maximum entropy method is applied in the energy spectrum computation for shorter wave trains. The use of shorter time windows does not reveal any significant variation in the tendency of Q to increase linearly with frequency as the length of the time window containing the sample of the S waves decreases. This seems to indicate that scattering-dependent Q is generally inseparable from intrinsic Q in the lithosphere when estimates based on variations with distance of the seismic signal spectrum are used. While the type of linear growth with frequency does not seem to undergo any variations (it remains of the Q = qf type), the data show there are a considerable decrease in the coefficient of proportionality Q with decreasing duration of the window of S waves analysed, probably as a result of variations in seismic attenuation with depth.     

On granitoid emplacement and related structures. A review

Granitoid magmas are emplaced at the upper crust under a complex interaction of gravitational processes and horizontal tectonics. Natural intrusive bodies show a wide variety of structural patterns that must be strongly related with their dynamic history of ascent and emplacement. Comparisons of natural structural patterns with experimental and numerical models are necessary to interpret in a coherent fashion the emplacement mechanism involved.From natural, experimental, numerical and theoretical considerations one can reach important conclusions on the problem of ascent and final emplacement of granitoid magmas in the Earth's crust. The present paper reviews the principal emplacement mechanisms referred to in the literature; that is, doming, diapirism, ballooning, stoping, cauldron subsidence and dike propagation.Dike propagation is the most effektive process in magma transport from deep zones in the crust and upper mantle. Extensional fractures for dike propagation and magma ascent can be developed at depth in the crust according to the modern dike propagation theory. In orogenic domains, magmas reach the upper crust through narrow channels or dikes and are accumulated in a final reservoir in the form of a discordant supracrustal pluton or a ballooning pluton if, during emplacement, any regional deformation acts simultaneously.

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Zusammenfassung Die Intrusion granitischer Magmen in die obere Krust ist das Ergebnis eines komplexen Zusammenspiels von schwerkraftbedingten Prozessen und horizontalen, tektonichen Bewegungen. Die gro\e Vielfalt tektonischer Strukturen von granitischen Plutonen spiegelt die Geschichte der Dynamik, ihres Aufstieges und ihrer Platznahme wider. Um den jeweils vorhandenen Intrusionsmechanismus zusammenhängend deuten zu können, sind Vergleiche der natürlichen, tektonischen Elemente mit experimentellen und numerischen Modellen notwendig. Hieraus lassen sich gegebenenfalls weitreichende Schlüsse zum Problem des Aufstiegs und der endgültigen Platznahme der Magmen in der Erkruste ziehen.In dieser Arbeit werden die wesentlichen Aufstiegsmechanismen von Magmen aus der Literatur diskutiert. Im Einzelnen sind dieses: Aufwölbung, Diapirismus, Aufweitung, Abbau, Kraterbildung und Gangentwicklung.Das Vordringen von Gängen ist der wirksamste Proze\ des Magmentransports aus tieferen Zonen der Kruste und des oberen Mantels. Ausdehnungsklüfte lassen sich als Ursache für das Vordringen von Gängen und den Magmenaufstieg nach der heutigen Theorie über die Entwicklung von Gängen in der tiefen Kruste herleiten. In orogenen Zonen erreichen Magmen die obere Erdkruste durch enge Kanäle oder Gänge und reichern sich dort auch in Form eines dikordanten, subkrustalen oder aufgweiteten Plutons an, wenn gleichzeitig mit der Platznahme regionaltektonische Deformationen ablaufen.

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Resumen Los magmas graníticos se emplazan en la corteza superior bajo una compleja interaccion entre procesos gravitatorios y tectónica horizontal. Los cuerpos intrusivos naturales muestran una amplia variedad de patrones estructurales que pueden estar directamente relacionados con la dinámica de ascenso y emplazamiento. Para explicar de forma cohérente el mecanismo de emplazamiento implicado en un plutón es necesario establecer comparaciones entre patrones estructurales de plutones y modelos experimentales y numéricos.A partir de consideraciones naturales, experimentales, numéricas y teóricas, se pueden extraer importantes conclusiones sobre el problema del ascenso y emplazamiento de magmas en la corteza. En este trabajo se revisan los principales mecanismos de emplazamiento referidos en la literatura; es decir, doming, diapirismo, ballooning, stoping, cauldron subsidence y propagación de diques.Propagación de diques es el proceso más efectivo en el transporte de magmas desde zonas profundas en la corteza y manto superior. De acuerdo con la moderna teoría de propagación de diques, las fracuras extensionales pueden producirse en profundidad en la corteza. En dominios orogénicos, los magmas alcanzan la corteza superior a través de estrechos canales o diques y se acumulan en un reservorio final, bien en forma de plutones discordantes supracrustales, o bien en la forma de un »ballooning pluton« si durante el emplazamiento actûa alguna deformación regional.

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Kinetics of reactions between aqueous sulfates and sulfides in hydrothermal systems

The rates of chemical reactions between aqueous sulfates and sulfides are essentially identical to sulfur isotopic exchange rates between them, because both the chemical and isotopic reactions involve simultaneous oxidation of sulfide-sulfur atoms and reduction of sulfate-sulfur. The rate of reaction can be expressed as a second order rate law: R = k·[∑SO₄^2?]·[∑S^2?], where R is the overall rate, k is the rate constant and [∑SO₄^2?] and [∑S^2?] are molal concentrations. We have computed the rate constants from the available experimental data on the partial exchange of sulfur isotopes between aqueous sulfates and sulfides using the rate law established by us: $\text{ln(}\text{α}{}^{\mathrm{e}}\text{? α}\text{α}{}^{\mathrm{e}}\text{? α}{}^0\text{) = ? kt([∑SO}{}_4{}^{\mathrm{2?}}\text{] + [∑S}{}^{\mathrm{2?}}\text{])}$, where t is time and α⁰, α, and α^e are, respectively, the fractionation factors at t = 0 (the initial condition), at the end of experiment, and at equilibrium. The equilibrium fractionation factor can be expressed as: $\text{1000 ln α}{}^{\mathrm{e}}\text{=}\text{6.463 × 10}{}^6\text{T}{}^2\text{+ 0.56 (±.5)}$ (T in Kelvin).The rate constants are strongly dependent on T and pH, but not in as simple a manner as suggested by Igumnov (1976). Our rate constants in Na-bearing hydrothermal solutions decrease by 1 order of magnitude with an increase in pH by 1 unit at pH's less than ~3, remain constant in the pH range of ~4 to ~7, and again decrease at pH >7. The activation energy for the reaction also depends on pH: 18.4 ± 1 kcal/mole at pH = 2, 29.6 ± 1 kcal/mole at pH = 4 to 7, and between 40 and 47 kcal/mole at pH around 9. The observed pH dependence of the rate constant and of the activation energy can be best explained by a model involving thiosulfate molecules as reaction intermediates, in which the intramolecular exchange of sulfur atoms in thiosulfates becomes the rate determining step.The rate constants obtained in this study were used to compute the changes in the isotopic fractionation factors between aqueous sulfates and sulfides during cooling of fluids. Comparisons with data of coexisting sulfate-sulfide minerals in hydrothermal deposits, suggest that simple cooling was not a likely mechanism for coprecipitation of sulfate and sulfide minerals at temperatures below 350°C. Mixing of sulfide-rich solutions with sulfate-rich solutions at or near the depositional sites is a more reasonable process for explaining the observed fractionation.The degree of attainment of chemical equilibrium between aqueous sulfates and sulfides in a hydrothermal system, and the applicability of a_O2-pH type diagrams to mineral deposits, depends on the ∑S content and the thermal history of the fluid, which in turn is controlled by the flow rate and the thermal gradient in the system.The rates of sulfate reduction by non-bacterial processes involving a variety of reductants are also dependent on T, pH, [∑SO₄^2?], and [∑S^2?], and appear to be fast enough to become geochemically important at temperatures above about 200°C.