Short-run Economic Benefits from Water Quality Improvements: an Application to the American Lobster (<Emphasis Type="Italic">Homarus Americanus</Emphasis>) Fishery of Long Island Sound

This article proposes a quantitative investigation of the claim that improving water quality does not yield rents in commercial fisheries that are inefficiently managed. Specifically, a combined model of the resource dynamics and fishing effort is used to investigate the effects of policy scenarios on water quality improvements on the American lobster fishery in Long Island Sound. Results indicate that short-run positive rents can be extracted from the lobster fishery even when inefficiently managed, but they dissipate in the long-run as suggested by the economic literature.     

Evolution of an early Eocene pull‐apart basin in the Central Pontides (Northern Turkey): New insights into the origin of the North Anatolian Shear Zone

Although the North Anatolian Shear Zone is one of the main lithospheric‐scale strike‐slip deformation zone in the world, playing a prominent role in the complex geodynamic interaction among the Eurasian, Anatolian and Arabian plates, the onset time of its activity remains highly controversial. Here, we tackle this issue by utilizing nannofossil biostratigraphy on deposits from the Ta?cilar basin, a pull‐apart basin that we have identified inside the North Anatolian Shear Zone overprinting the Intra‐Pontide suture zone. The syn‐tectonic sedimentary succession of the Ta?cilar basin developed completely during the early Eocene (Ypresian; CNE4–CNE5 Zones). The strike‐slip faulting related to the initial onset of the North Anatolian Shear Zone can likely be constrained within the Ypresian, suggesting that the westward escape of the Anatolian plate along the North Anatolian Shear Zone started in the early Eocene.     

High-<Emphasis Type="Italic">T</Emphasis> behaviour of gedrite: thermoelasticity,cation ordering and dehydrogenation

The thermoelastic behaviour of a natural gedrite having the crystal-chemical formula ^ANa_0.47 ^B(Na_0.03 Mg_1.05 Fe_0.86²⁺ Mn_0.02 Ca_0.04) ^C(Mg_3.44 Fe_0.36²⁺ Al_1.15 Ti_0.05⁴⁺) ^T(Si_6.31 Al_1.69)O₂₂ ^W(OH)₂ has been studied by single-crystal X-ray diffraction to 973 K (Stage 1). After data collection at 973 K, the crystal was heated to 1,173 K to induce dehydrogenation, which was registered by significant changes in unit-cell parameters, M1–O3 and M3–O3 bond lengths and refined site-scattering values of M1 and M4 sites. These changes and the crystal-chemical formula calculated from structure refinement show that all Fe²⁺ originally at M4 migrates into the ribbon of octahedrally coordinated sites, where most of it oxidises to Fe³⁺, and there is a corresponding exchange of Mg from the ribbon into M4. The resulting composition is that of an oxo-gedrite with an inferred crystal-chemical formula ^ANa_0.47 ^B(Na_0.03 Mg_1.93 Ca_0.04) ^C(Mg_2.56 Mn_0.02²⁺ Fe_0.10²⁺ Fe_1.22³⁺ Al_1.15 Ti_0.05⁴⁺) ^T(Si_6.31 Al_1.69) O₂₂ ^W[O_1.12²⁻ (OH)_0.88]. This marked redistribution of Mg and Fe is interpreted as being driven by rapid dehydrogenation at the H3A and H3B sites, such that all available Fe in the structure orders at M1 and M3 sites and is oxidised to Fe³⁺. Thermoelastic data are reported for gedrite and oxo-gedrite; the latter was measured during cooling from 1,173 to 298 K (Stage 2) and checked after further heating to 1,273 K (Stage 3). The thermoelastic properties of gedrite and oxo-gedrite are compared with each other and those of anthophyllite.     

Holocene palaeohydrological changes in the northern Mediterranean borderlands as reflected by the lake-level record of Lake Ledro,northeastern Italy

A lake-level record of Lake Ledro (northern Italy) spans the entire Holocene with a chronology derived from 51 radiocarbon dates. It is based on a specific sedimentological approach that combines data from five sediment profiles sampled in distinct locations in the littoral zone. On a millennial scale, the lake-level record shows two successive periods from 11,700 to 4500 cal yr BP and from 4500 cal yr BP to the present, characterized by lower and higher average lake levels, respectively. In addition to key seasonal and inter-hemispherical changes in insolation, the major hydrological change around 4500 cal yr BP may be related to a non-linear response of the climate system to orbitally-driven gradual decrease in insolation. The Ledro record questions the notion of an accentuated summer rain regime in the northern Mediterranean borderlands during the boreal insolation maximum. Moreover, the Ledro record highlights that the Holocene was punctuated by successive centennial-scale highstands. Correlations with the Preboreal oscillation and the 8.2 ka event, and comparison with the atmospheric ¹⁴C residual record, suggest that short-lived lake-level fluctuations developed at Ledro in response to (1) final steps of the deglaciation in the North Atlantic area and (2) variations in solar activity.     

Local structural relaxation around Co2+ along the hardystonite–Co-?kermanite melilite solid solution

Six pure compounds belonging to the hardystonite (Ca₂ZnSi₂O₇)–Co-?kermanite (Ca₂CoSi₂O₇) solid solution were investigated by the combined application of X-ray powder diffraction and electronic absorption spectroscopy. Structural refinements of the XRPD data revealed a negative excess volume of mixing due to the single isovalent substitution of Co for Zn in the tetrahedral site. In agreement with the diffraction data, deconvolution of the optical spectra showed a progressive decreasing of the crystal field strength parameter 10Dq moving toward the Co-?kermanite end-member, meaning that the local cobalt–oxygen bond distance, $ \langle {\text{Co}}{-}{\text{O}}\rangle^{\text{local}} $ , increased along the join with the amount of cobalt. The calculated structural relaxation coefficient around the fourfold coordinated Co²⁺ in the Ca₂(Zn_1?x Co _x )Si₂O₇ join was ε?=?0.69, very far from the one predicted by the Vegard’s law (ε?=?0) and at variance with ε?=?0.47 previously found for tetrahedrally coordinated Co²⁺ in gahnite–Co-aluminate spinel solid solution. This difference is consistent with the largest constraints existing on the spinel structure, based on cubic closest packing, compared to the more flexible layered melilite structure.     

Melilite-type and melilite-related compounds: structural variations along the join Sr2?xBaxMgSi2O7 (0?≤?x?≤?2) and high-pressure behavior of the two end-members

The structural variations along the solid solution Sr_2−x Ba _x MgSi₂O₇ (0 ≤ x ≤ 2), combined to the high-pressure characterization of the two end-members, have been studied. A topological change from the tetragonal (melilite-type) to the monoclinic (melilite-related) structure along the join Sr₂MgSi₂O₇ (e.g., P[`4]2₁ m P\bar{4}2_{1} m )–Ba₂MgSi₂O₇ (e.g., C2/c) occurs with a Ba content higher than 1.6 apfu. Favored in the crystallization from a melt, the tetragonal form has a tetrahedral sheet topology exclusively based on five-membered rings, which provide a regular “4 up + 4 down” ligand arrangement. In contrast, the melilite-related structure, favored by solid-state reaction synthesis, is made by alternating six- and four-membered tetrahedral rings, which give an asymmetric arrangement of alternated “5 up + 3 down” and “3 up + 5 down” ligands around Sr or Ba. This latter configuration is characterized by an additional degree of freedom with Ba polyhedra hosted in the interlayer with a more irregular and compact coordination and longer Ba–O bond distances. Further insights into the relationships between the two melilite typologies were achieved by investigating the in situ high-pressure behavior of these systems. The synchrotron high-pressure experiments allowed to calculate the elastic moduli for the Sr melilite-type end-member and for the Ba monoclinic polymorph (Sr₂MgSi₂O₇: K _T0 = 107, K _a=b  = 121, and K _c  = 84 GPa; m-Ba₂MgSi₂O₇: K _T0 = 85, K _a  = 96, K _b  = 72, and K _c  = 117 GPa) and compare them with those reported in the literature for ?kermanite (Ca₂MgSi₂O₇). The results show that, although the volume of Ba polyhedron in tetragonal polymorphs is larger than in the monoclinic forms, the interlayer compressibility is significantly lower in the former structures due to the occurrence of very short Ba–O distances. This unfavored Ba environment also makes tetragonal Ba₂MgSi₂O₇ a metastable phase at room conditions, possibly favored by high pressure. However, no phase transition occurs from monoclinic to tetragonal form due to kinetic hindrance in reconstructing the sheet topology.     

Genesis of the hydrothermal gold deposits in the Canan area,Lepaguare District,Honduras

The Canan area (Honduras) is characterized by a gold-bearing ore deposit that is associated with quartz-veined shear zones. Gold mineralization occurs in low-to medium-grade metamorphic host-rocks (graphitic and sericitic schists). Hydrothermal fluids, which are associated with the emplacement of Cretaceous-Tertiary granodioritic intrusions, are responsible for the formation of quartz veins and the hydrothermal alteration of wall-rocks. Three main altered zones have been detected in the wall-rocks as far as 150 cm from the quartz veins. The distal zone (up to 50-cm thick) contains quartz, chlorite and illite. The intermediate zone is the thickest (up to 80 cm) and is marked by quartz, muscovite, sulphides, kaolinite and native elements such as Au and Ag. The proximal zone, which is close to the quartz veins, is rather thin (up to 25 cm) and contains clay minerals, Al-oxides-hydroxides and sulphides. The transition from the distal to the proximal zone is accompanied by the enrichment of SiO₂ and the depletion of all other major elements, except for Fe₂O_3(tot). Precious metals occur in the highest concentrations in the intermediate zone (Au up to 7.6 ppm and Ag up to 11 ppm). We suggest that gold was transported as a reduced sulphur complex and was precipitated from the hydrothermal solution by the reaction of the sulphur complexes with Fe²⁺ from the alteration of the mafic minerals of the host-rock. Fluid–wall-rock interactions seem to be the main cause of gold mineralization. Genetic relationships with a strike-slip fault system, hydrothermal alteration zones within the metamorphic wall-rocks, and an entire set of geochemical anomalies are consistent with orogenic-type gold deposits of the epizonal class.     

HVSR technique as tool for thermal-basin characterization: a field example in N-E Italy

The Euganean thermal basin, located in the Eastern Po plain (Italy), is one of the most important thermal districts of Italy (Euganean–Berician Thermal District). The presence of hot water in the basin has brought about its exploitation over time. The thermal area has been known since the Roman Empire and is still of crucial interest for the profitable use of its hydro-geological resources. For these reasons the water cycle of the thermal area has been thoroughly studied, in particular with regard to its chemical and hydrogeological properties. The effects of well pumping, such as subsidence and water temperature steadiness, have been monitored over time. In the present work, the Horizontal to Vertical Spectral Ratio (HVSR) single station microtremor technique was applied as a non-invasive geophysical tool for the characterization of a part of the Euganean–Berician thermal district involving the municipalities of Abano and Montegrotto towns. This study represents the first correlation between the results from microtremor geophysical surveys and the thermal basin geological structure, including remote sensing data and thermal well information. More than 50 HVSR measurements from single stations were collected and analysed, in close correlation with the vast amount of available borehole logs, well exploitation data and SAR interferometry measurements collected for the monitoring of land subsidence induced by thermal water pumping. The aim of the work was to evaluate the suitability of the microtremor technique for the preliminary characterization of a thermal basin, in terms of resonance properties of the alluvial deposits covering the rocky bedrock, evaluated by means of HVSR methods. HVSR results were interpreted in terms of regional geological setting and hydrogeological properties of the subsoil. Our field results confirmed the existence of significant correlations between the resonance behaviour of the basin determined by the HVSR technique and the geological structures, suggesting that single station measurements are a promising tool for creating a rapid and preliminary non-invasive contribution to the characterization of the geothermal basin.     

Natural Cr(VI) contamination of groundwater in the Cecina coastal area and its inner sectors (Tuscany,Italy)

A detailed hydrogeochemical study of groundwater in the Cecina coastal plain (Livorno province, Italy) and its inner sectors was undertaken in 2008, as chemical analyses carried out on groundwater since 2006 have revealed Cr(VI) concentrations of up to 49 μg/L (well above the permissible limit of 5 μg/L). Ophiolite outcrops are present throughout the study area, and their fragments likely represent a significant portion of the existing multilayered aquifer skeleton. Waters delivered by the serpentinite outcrops have a typically Mg–HCO₃ composition, whereas those of the coastal plain are prevailingly of the Ca/Mg–HCO₃ type with significant Mg contents. Significant NO₃ contamination characterises the studied coastal plain, and an interesting negative correlation exists between Cr(VI) and both NO₃ and SO₄ deriving from the widespread use of (NH₄)₂SO₄ as a farm fertilizer. Chromium speciation calculations carried out using the EQ3NR code reveal that the prevailing Cr(VI) species in solution is CrO₄ ^2?; however, CaCrO₄° and MgCrO₄° neutral complexes represent significant percentages (up to 42 %). These findings suggest that the mobility and consequently the bioavailability of Cr(VI) can be significantly enhanced by these neutral complexes, which are not considered to be affected by adsorption/desorption processes. The Cr(VI) source, investigated by means of the Mg/SiO₂ molar ratio, seems to be represented mainly by Mg-bearing minerals of the chlorite group. Petrographic observations confirm the occurrence of this mineral group. The interaction between rainwater and the local serpentinite rock was simulated at different $P_{{{\text{CO}}_{ 2} }}$ and $P_{{{\text{O}}_{ 2} }}$ conditions by reaction path modelling using the EQ3/6 software package. $P_{{{\text{O}}_{ 2} }}$ was varied in accordance with the assumption that redox conditions are determined in part by NO₃. Results are in good agreement with experimental data on spring waters and subordinately with data on some coastal plain groundwater, which plot in a rather wide $P_{{{\text{CO}}_{ 2} }}$ and $P_{{{\text{O}}_{ 2} }}$ field. Although the dissolved Cr content is mostly of natural origin, fertilization may affect its fate.