25 research outputs found
Are Taxonomic Distinctness measures compliant to other ecological indicators in assessing ecological status?
Assessing the ecological status, a concept implemented in the European Water Framework Directive [EC, 2000. Directive of the European Parliament and of the Council 2000/60/EC establishing a framework for community action in the field of water policy PE-CONS 3639/1/00, p. 72], requires the application of methods capable of distinguishing different levels of ecological quality. The Average Taxonomic Distinctness has been used as tool in this context, and we tested the robustness of Taxonomic Distinctness measures applying it in different scenarios (estuarine eutrophication, organic pollution, and re-colonisation after physical disturbance), analysing simultaneously its compliance to other types of ecological indicators. Results show that, in most of the case studies, only Total Taxonomic Distinctness was relatively satisfactory in discriminating between disturbed situations. Other Taxonomic Distinctness measures have not proved to be more sensitive than other ecological indicators (Shannon-Wiener, Margalef, and Eco-Exergy indices). Therefore, this approach does not seem to be particularly helpful in assessing systems' ecological status with regard to the WFD implementation.http://www.sciencedirect.com/science/article/B6V6N-4KHK1M9-3/1/e54484859b25163a57c5780ac3bf46c
Microstructure and secondary phases in coevaporated CuInS2 films: Dependence on growth temperature and chemical composition
The microstructure of CuInS2-(CIS2) polycrystalline films deposited onto Mo-coated glass has been analyzed by Raman scattering, Auger electron spectroscopy (AES), transmission electron microscopy, and x-ray diffraction techniques. Samples were obtained by a coevaporation procedure that allows different Cu-to-In composition ratios (from Cu-rich to Cu-poor films). Films were grown at different temperatures between 370 and 520-°C. The combination of micro-Raman and AES techniques onto Ar+-sputtered samples has allowed us to identify the main secondary phases from Cu-poor films such as CuIn5S8 (at the central region of the layer) and MoS2 (at the CIS2/Mo interface). For Cu-rich films, secondary phases are CuS at the surface of as-grown layers and MoS2 at the CIS2/Mo interface. The lower intensity of the MoS2 modes from the Raman spectra measured at these samples suggests excess Cu to inhibit MoS2 interface formation. Decreasing the temperature of deposition to 420-°C leads to an inhibition in observing these secondary phases. This inhibition is also accompanied by a significant broadening and blueshift of the main A1 Raman mode from CIS2, as well as by an increase in the contribution of an additional mode at about 305 cm-1. The experimental data suggest that these effects are related to a decrease in structural quality of the CIS2 films obtained under low-temperature deposition conditions, which are likely connected to the inhibition in the measured spectra of secondary-phase vibrational modes
Are Taxonomic Distinctness measures compliant to other ecological indicators in assessing ecological status?
Assessing the ecological status, a concept implemented in the European Water Framework Directive [EC, 2000. Directive of the European Parliament and of the Council 2000/60/EC establishing a framework for community action in the field of water policy PE-CONS 3639/1/00, p. 72], requires the application of methods capable of distinguishing different levels of ecological quality. The Average Taxonomic Distinctness has been used as tool in this context, and we tested the robustness of Taxonomic Distinctness measures applying it in different scenarios (estuarine eutrophication, organic pollution, and re-colonisation after physical disturbance), analysing simultaneously its compliance to other types of ecological indicators. Results show that, in most of the case studies, only Total Taxonomic Distinctness was relatively satisfactory in discriminating between disturbed situations. Other Taxonomic Distinctness measures have not proved to be more sensitive than other ecological indicators (Shannon-Wiener, Margalef, and Eco-Exergy indices). Therefore, this approach does not seem to be particularly helpful in assessing systems' ecological status with regard to the WFD implementation.http://www.sciencedirect.com/science/article/B6V6N-4KHK1M9-3/1/e54484859b25163a57c5780ac3bf46c
Genetic differentiation and gene flow of two sparidae subspecies, Diplodus sargus sargus and Diplodus sargus cadenati in Atlantic and south-west Mediterranean populations
A total of nine enzymes coded by 14 loci were assayed for each of six populations (from the north-eastern Atlantic and the Mediterranean) of two sea bream subspecies (Diplodus sargus sargus and Diplodus sargus cadenati). Diagnostic alleles were observed for each subspecies, although there were several common alleles. Estimates of variance in allele frequencies among samples (FST) revealed significant differences (P<0.05) among both subspecies. Genetic divergence was found between Atlantic and Mediterranean samples: values for genetic distances were higher than 0.163. Furthermore, D. sargus cadenati populations displayed a higher mean weight and length than D. sargus sargus populations and significant differences in growth were found among subspecies and populations. These results are discussed in terms of levels of gene flow and its respective relationships with water circulation in the Strait of Gibraltar and geological events.info:eu-repo/semantics/publishedVersio
Genetic differentiation of Diplodus sargus (Pisces: Sparidae) populations in the south-west Mediterranean
Allozyme analysis of tissue samples of 1249 white sea bream Diplodus sargus from five localities of the south-west
Mediterranean revealed a high degree of genetic polymorphism. The observed heterozygosity ranged from 0.4182
(Cape of Palos) to 0.3138 (Tabarca). Several populations were characterized by unique alleles. Examination of the
spatial structure was performed using Neiâs distances and F-statistics, and indicated genetic differences between
groups. One group, which clustered Tabarca and Guardamar, could be explained by the small geographical distance
between them. MazarrĂłn and Cape of Palos samples showed genetic divergence from other samples (Guardamar,
Tabarca and Ăguilas) and this difference may be as a result of local current systems and larval dispersal.info:eu-repo/semantics/publishedVersio
Temporal genetic variation in populations of Diplodus sargus from the SW Mediterranean Sea
Population genetic studies on white sea bream Diplodus sargus have revealed different
patterns in the subdivision of populations in the Mediterranean Sea. However, the stability of
observed allele frequencies over time remains poorly tested. The aim of this study was to show that
the genetic structure of D. sargus could significantly change over time by analysing temporal variations
in allozymes. In order to determine temporal variation in the genetic structure of 5 natural
D. sargus populations in the SW Mediterranean, we screened 14 allozyme loci. Our main finding was
the significant genotypic differentiation among cohorts (year-classes) in the Guardamar (FST = 0.012;
p < 0.001) and Cape of Palos (FST = 0.008; p < 0.001) populations. The differentiation observed in the
present study when considering pair-wise comparisons between cohorts is similar to that of all populations
throughout the Mediterranean Sea. Our results suggest that microgeographical variations,
also known as âchaotic genetic patchinessâ, could occur in D. sargus populations from the SW
Mediterranean. The recruitment of genetically variable cohorts at 1 site each year may account for
these variations. We also discussed alternative explanations for this genetic pattern. This study confirms
the importance of understanding the ecology, behaviour and environment of fish populations
when investigating population genetic structure. Our results also highlight the importance of incorporating
temporal samples when conducting population structure studies.info:eu-repo/semantics/publishedVersio