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We aim to show how some of the important interdisciplinary fixes or solutions to diverse problems observed in fisheries can complement each other. This can be achieved through methodical allocation of the rights pertaining to fisheries and simultaneous implementation of policy instruments to correct for market failures and equity concerns. We emphasize via a roadmap that there are some general principles that should be invoked when choosing between alternative structures of rights. Our examples from Sweden provide evidence of the flexibility of fishing rights and how they can be adapted to integrate fixes from different disciplines into practical fisheries management. 相似文献
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Broadly speaking, there is, at least within geomorphic circles, a general acceptance that rocks with low albedos will warm both faster and to higher temperatures than rocks with high albedos, reflectivity influencing radiative warming. Upon this foundation are built notions of weathering in respect of the resulting thermal differences, both at the grain scale and at the scale of rock masses. Here, a series of paving bricks painted in 20 per cent reflectivity intervals from black through to white were used to monitor albedo‐influenced temperatures at a site in northern Canada in an attempt to test this premise. Temperatures were collected, for five months, for the rock surface and the base of the rock, the blocks being set within a mass of local sediment. Resulting thermal data did indeed show that the dark bricks were warmer than the white but only when their temperatures were equal to or cooler than the air temperature. As brick temperature exceeded that of the air, so the dark and light bricks moved to parity; indeed, the white bricks frequently became warmer than the dark. It is argued that this ‘negating’ of the albedo influence on heating is a result of the necessity of the bricks, both white and black, to convect heat away to the surrounding cooler air; the darker brick, being hotter, initially convects faster than the white as a product of the temperature difference between the two media. Thus, where the bricks become significantly hotter than the air, they lose energy to that air and so their respective temperatures become closer, the albedo influence being superceded by the requirement to equilibrate with the surrounding air. It is argued that this finding will have importance to our understanding of weathering in general and to our perceptions of weathering differences between different lithologies. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
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Dan-Erik Lindberg Kjell Leonardsson Anders G. Andersson T. Staffan Lundström Hans Lundqvist 《Limnologica》2013,43(5):339-347
The spatial distribution of upstream migrating Atlantic salmon (Salmo salar) spawners was studied in 2008 and 2009 in the surroundings of the tailrace from a hydropower station in the River Umeälven. This area is problematic because the fish have difficulties finding their way into the original riverbed, which prompted an investigation on the feasibility of adding a fishway in the area. Echo sounding was used in 2008 to investigate the spatial use of fish in the tailrace channel during the time of salmon migration. Presence of other fish species was so low that all echo sounding detections were assumed to be salmon. In 2009, data on wild radio-tagged salmon (n = 94) was collected in the same tailrace by an array of underwater antennas with a detection radius of approximately 10 m, to validate the results from the echo sounding. Both types of surveys showed aggregations of fish in one part of the tailrace. As a final step, Computational Fluid Dynamics (CFD) modeling was performed to analyze hydrodynamics. This CFD modeling showed a coincidence of fish detections in areas with turbulence intensities between 0.6 and 0.8, which may be an indication that the fish are holding in these areas to reduce energy expenditure during migration. A high proportion of the radio-tagged salmon were observed in the tailrace area (a median of 21 days between their first and last detection), indicating that the salmon are delayed in their upstream migration by the attraction to the tailrace in this area. The overall data on fish behavior in the tailrace led us to suggest a location for a new fishway where the fish aggregation was most pronounced. The number of detections from either technology had similar distributions over the tailrace, suggesting that the results are comparable. Thus, the split beam echo sounder can preferably be used to investigate which location is most appropriate for locations of entrances to new fishways since many more individual fishes are covered by this method compared to telemetry. Furthermore, there is no need to handle the fish in the echo sounding studies as is required in telemetry studies. 相似文献
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Veronika Gälman Johan Rydberg Andrei Shchukarev Staffan Sjöberg Antonio Martínez-Cortizas Richard Bindler Ingemar Renberg 《Journal of Paleolimnology》2009,42(1):141-153
Easily discernible sediment varves (annual laminations) may be formed in temperate zone lakes, and reflect seasonal changes in the composition of the accumulating material derived from the lake and its catchment (minerogenic and organic material). The appearance of varves may also be influenced by chemical processes. We assessed the role of iron (Fe) and sulfur (S) in the appearance of varves in sediments from Lake Nylandssjön in northern Sweden. We surveyed Fe in the lake water and established whether there is internal transport of Fe within the sediment. We used a unique collection of seven stored freeze cores of varved sediment from the lake, collected from 1979 to 2004. This suite of cores made it possible to follow long-term changes in Fe and S in the sediment caused by processes that occur in the lake bottom when the sediment is ageing. We compared Fe and S concentrations using X-ray fluorescence spectroscopy (XRF) in specific years in the different cores. No diagenetic front was found in the sediment and the data do not suggest that there is substantial vertical transport of Fe and S in the sediment. We also modeled Fe and S based on thermodynamic, limnological, and sediment data from the lake. The model was limited to the five components H+, e?, Fe3+, SO4 2?, H2CO3 and included the formation of solid phases such as Fe(OH)3 (amorphous), FeOOH (aged, microcrystalline), FeS and FeCO3. Modeling showed that there are pe (redox) ranges within which either FeS or Fe(OH)3/FeOOH is the only solid phase present and there are pe ranges within which the two solid phases co-exist, which supports the hypothesis that blackish and grey-brownish layers that occur in the varves were formed at the time of deposition. This creates new possibilities for deciphering high-temporal-resolution environmental information from varves. 相似文献
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The apparent ionization constants for silicic acid, k1 and k2, and the ionic product of water, kw, have been determined in 0.05, 0.1, 0.2, 0.4 and 2.0 M Na(CI) media at 25°C. The medium dependence of these constants was found to fit equations of the form where K1 is the ionization constant in pure water, αi and bi are parameters of which bi has been adjusted to present data. The following results were obtained (αi, bi): pK1 = 9.84, (1.022, ?0.11); pK2 = 13.43, (2.044, ?0.20); and pKw = 14.01 (1.022, ?0.22). ki values are collected in Tables I and II. Attempts have been made to explain the medium dependence of k1 and k2 with weak sodium silicate complexing according to the equilibria giving k11 = 0.37M?1 and k21= 3.0M?1. However, these weak interactions cannot be interpreted unambiguously from potentiometric data at different 1-levels. Probably the medium dependence could equally well be expressed by variations in the activity coefficients.The measurements were performed as potentiometric titrations using a hydrogen electrode. The average number of OH- reacted per Si(OH)4, Z, has been varied within the limits 0 ? Z ? 1.1 and B1, the total concentration of Si(OH)4, between 0.001 M and 0.008 M. k1 was evaluated from experimental data with B ? 0.003 M, and k2 with B ? 0.008 M and Z ? 0.95. 相似文献
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Åsa Bengtsson Andrei Shchukarev Per Persson Staffan Sjöberg 《Geochimica et cosmochimica acta》2009,73(2):257-259
The dissolution and surface complexation of a non-stoichiometric hydroxyapatite (Ca8.4(HPO4)1.6(PO4)4.4(OH)0.4), (HAP) was studied in the pH range 3.5-10.5, at 25 °C in 0.1 M Na(Cl). The results from well-equilibrated batch experiments, potentiometric titrations, and zeta-potential measurements were combined with information provided by Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy and X-ray Photoelectron Spectroscopy (XPS). The information from the analyses was used to design an equilibration model that takes into account dissolution, surface potential, solution and surface complexation, as well as possible phase transformations. The results from the XPS measurements clearly show that the surface of the mineral has a different composition than the bulk and that the Ca/P ratio of the surface layer is 1.4 ± 0.1. This ratio was also found in solution in the batches equilibrated at low pH where the dominating reaction is dissolution. In the batches equilibrated at near neutral pH values, however, the Ca/P ratio in solution attains values as high as 25, which is due to re-adsorption of phosphate ions to the HAP surface. The total concentration of protons as well as the total concentration of dissolved calcium and phosphate in solution were used to calculate a model for the dissolution and surface complexation of HAP. The constant capacitance model was applied in designing the following surface complexation model:
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The complexation of Cd(II) and Cd(II)-phthalate at the goethite/water interface were investigated by EXAFS and IR spectroscopy, by batch adsorption experiments and by potentiometric titrations at 298.15 K. The EXAFS spectra showed Cd(II) to form only inner-sphere corner-sharing complexes with the goethite surface sites in the presence and absence of phthalate. EXAFS spectra also showed the presence of Cd(II)-chloride complexes in 0.1 mol/L NaCl. IR spectra also showed phthalate to form (1) an inner-sphere complex with adsorbed corner-sharing Cd(II) surface complexes in the pH 3.5 to 9.5 and (2) an outer-sphere complex with the same type of corner-sharing Cd(II) complex however at pH > 6, in addition to the inner- and outer-sphere complexes of phthalate reported in a previous study. The potentiometric titration and the batch adsorption data were used to constrain the formation constants of the different Cd(II)-phthalate surface complexes on the dominant {110} and the {001} planes of the goethite. The models were carried out with the Charge Distribution Multisite Complexation model coupled to the Three Plane Model and can predict the molecular-scale speciation of cadmium and phthalate in the presence of goethite. Cd(II) adsorption models calibrated on a 90 m2/g goethite also could accurately predict experimental data for a 37 m2/g goethite of slightly different basic charging properties. 相似文献
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The objective of this study was to describe the proton promoted disproportion of synthetic manganite (γ-MnOOH) and to characterise
the resulting phase transformations. The solution and remaining solid phase after disproportionation was analysed by techniques
including atomic absorbance spectroscopy, X-ray diffraction (XRD), atomic force microscopy (AFM) and scanning electron microscopy
(SEM). In suspensions with pH between 5 and 7, −log[H+] was monitored for 17 months and equilibrium constants were determined at 9, 12 and 17 months of reaction time for the following
reaction (25 °C, 0.1 M (Na)NO3):
The formed MnO2 ages with time and the equilibrium constant for a metastable phase (ramsdellite or nsutite) as well as the most stable phase,
pyrolusite (β-MnO2), was determined. Furthermore, combined pH and pe (Eh) measurements were performed to study the equilibrium;
Real-time AFM measurements of the dissolution showed shrinkage of the length of the manganite needles with time (2 hours).
After 1 week SEM images showed that this decreased length also was followed by a reduced thickness of the manganite needles.
From the SEM images the morphology of the formed Mn(IV) oxides was studied. At pH 2.6, pyrolusite (β-MnO2) and MnCl2 were found in the XRD patterns. Throughout the pH range there were indications of ramsdellite (MnO1.97) in the XRD patterns, which coincided with the existence of a fraction of needle shaped crystals with smaller dimensions
(compared to manganite) in the SEM images. These observations together with the long term dissolution experiments suggest
that the dissolution of manganite initially forms a ramsdellite or nsutite phase that over time rearranges to form pyrolusite. 相似文献