Green areas and water management in residential developments in the European Western Mediterranean. A case study of Alicante,Spain

The intense urbanization of the Mediterranean coast as a result of the development of residential-tourist activities since the 1960s, especially from the mid-1990s to 2008, has generated new urban environments associated with extensive urban typologies. These include gardens linked to houses with outdoor spaces that are shared between all of the residents of the residential developments. The aim of this study is to determine the main characteristics of these new urban green spaces and their effect on domestic water consumption in Alicante (Spain). To do this, we analysed the characteristics that define these types of gardens (surface area, density, plant species and irrigation system) and determined their water needs using the Water Use Classifications of Landscape Species method. The main conclusions are that the increase in paved areas is one of the strategies to reduce water consumption in spaces where turf grass is the most common plant species. This is due to increased water prices and lack of water resources.     

Thermal stability of extended clusters in dravite: a combined EMP,SREF and FTIR study

A dravite from Yemen of near end-member composition was treated in air and hydrogen atmospheres at 600–900 °C to reveal changes in Mg and Al order over the octahedrally coordinated Y and Z sites, and to explore related changes in the characteristic vibrational bands in the principal (OH)-stretching frequency. Relevant information was obtained using electron microprobe analysis (EMPA), structural refinement (SREF) and polarized infrared (IR) single-crystal spectroscopy. Overall, the EMPA, SREF and IR data show that only minor changes occur during thermal treatment up to at least 800 °C, including variations in structural parameters, Mg–Al order–disorder and (OH)-stretching bands, indicating limited hydrogen loss. Untreated and treated dravite samples have very similar long-range and short-range atomic structures, which may be related to the occurrence of stable Al–Mg extended clusters around the O1 (=W) and O3 (=V) sites: ^W(F)–^Y(MgMgMg)–^V(OH)₃–^Z[AlAlAlAlAl(Al,Mg)]; ^W(OH)–^Y(MgMgAl)–^V(OH)₃–^Z[AlAlAlAlAl(Al,Mg)]; ^W(O^2–)–^Y(AlAlAl)–^V(OH)₃–^Z[AlAlAlAlAl(Al,Mg)]. These extended clusters remain stable to temperatures close to the observed start of decomposition (~900 °C).     

A method for estimating microporosity of fine‐grained sediments and sedimentary rocks via scanning electron microscope image analysis

This study presents a method of two‐dimensional scanning electron microscope image analysis that directly quantifies microporosity abundance in clay‐rich, fine‐grained sediments. The method is novel in that it is specifically designed to circumvent the challenge to porosity quantification posed by mineral surface charging and topographical artifacts created during Ar‐ion cross‐section polishing. It utilizes the finding that differences in circularity values can be used to distinguish micropores from blemishes in a thresholded image. This method is powerful because it is fast and provides a direct microporosity estimation technique to augment or replace experimental data. The pore size range to which the method is applicable is clear and can be selected depending on the application of the analysis. When used appropriately, the method can be implemented on microporous sediments and sedimentary rock in general. The method is developed using marine muds of Pliocene and Miocene ages from the Nankai margin (burial depths from approximately 200 to 1100 m). The close match between imaging‐derived microporosity and bulk N₂ microporosity measurements shows that porosity in these young and relatively shallowly buried sediments is dominated by pores of sizes that can be imaged by scanning electron microscopy. In Kumano, forearc basin sediments of the Nankai Trough, results of this method show a significant increase in microporosity with burial depth, probably due to microporosity preservation during compaction and possibly early volcanic ash diagenesis.     

Geochemical mobility of arsenic in the surficial waters from Argentina

The presence of arsenic (As) in surface water constitutes an important environmental risk, where mobility and adsorption processes are responsible for its behavior in the sediment–water interface. Therefore, the assessment of adsorption, mobility and water availability of arsenic in freshwater sediments, with agricultural, livestock and urban soil uses was performed. Arsenic concentrations in sediments ranged from 5.4 to 15.9 mg kg^?1 (total) and 2.8 to 6.5 mg kg^?1 (labile), and those of iron and manganese were 11,563–23,500 and 140.6–662.1 mg kg^?1, respectively. The As levels in water were significantly lower than those of sediments. Results would suggest that As co-precipitation and adsorption on Fe oxides are probably the major route of immobilization, determining its low lability. Manganese did not present an outstanding contribution to the retention, and cation-exchange capacity, pH and organic matter of sediments did not show an influence on the mobility of As.