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Authors = João Machado

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Open AccessArticle Engaging Citizen Participation—A Result of Trusting Governmental Institutions and Politicians in the Portuguese Democracy
Soc. Sci. 2016, 5(3), 40; doi:10.3390/socsci5030040
Received: 8 May 2016 / Revised: 26 July 2016 / Accepted: 27 July 2016 / Published: 5 August 2016
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Abstract
Public participation is a mainstay of democracy. However, the ways in which it can be understood inevitably influence the achievement of the goals that preside over any public policy. Literature argues that the drawbacks of citizen participation are directly related to the level
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Public participation is a mainstay of democracy. However, the ways in which it can be understood inevitably influence the achievement of the goals that preside over any public policy. Literature argues that the drawbacks of citizen participation are directly related to the level of trust in governmental institutions and in politicians. The present study was carried out on a sample of 250 individuals and aimed to (1) describe citizens’ opinions and trust in politicians and government institutions; and (2) demonstrate that healthy levels of citizen engagement in politics may be upheld as long as citizens trust their political institutions and leaders, through a case study of Portugal’s democratic system. The current study found no statistically significant association between political participation and the study participant’s perception that government representatives heard (p = 0.769) or considered (p = 0.810) their opinions. Similarities were found between the participants’ assessments of the quality of life brought about by the decisions of those in power and the levels of citizen participation around land planning and land management (p = 0.011). Also, citizen assessments of life quality were influenced by their understanding of political decisions (p = 0.014). Effective communication between citizens and politicians will allow both to better understand the aims of political policy. When citizens believe that politicians are honest, show moral leadership and demonstrate integrity, and that these values are upheld by public institutions, a common aspiration can be realized: improving the quality of life. Full article
Open AccessArticle Culture-Independent Study of the Late-Stage of a Bloom of the Toxic Dinoflagellate Ostreopsis cf. ovata: Preliminary Findings Suggest Genetic Differences at the Sub-Species Level and Allow ITS2 Structure Characterization
Toxins 2015, 7(7), 2514-2533; doi:10.3390/toxins7072514
Received: 26 March 2015 / Revised: 6 June 2015 / Accepted: 24 June 2015 / Published: 30 June 2015
Cited by 1 | Viewed by 1126 | PDF Full-text (1822 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Available genomic data for the toxic, bloom-forming, benthic Ostreopsis spp. are traditionally obtained from isolates rather than from individuals originally present in environmental samples. Samples from the final phase of the first reported Ostreopsis bloom in European North Atlantic waters (Algarve, south coast
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Available genomic data for the toxic, bloom-forming, benthic Ostreopsis spp. are traditionally obtained from isolates rather than from individuals originally present in environmental samples. Samples from the final phase of the first reported Ostreopsis bloom in European North Atlantic waters (Algarve, south coast of Portugal) were studied and characterized, using a culture-independent approach. In the first instance, a microscopy-based analysis revealed the intricate complexity of the samples. Then, we evaluated the adequacy of commonly used molecular tools (i.e., primers and nuclear ribosomal markers) for the study of Ostreopsis diversity in natural samples. A PCR-based methodology previously developed to identify/detect common Ostreopsis species was tested, including one new combination of existing PCR primers. Two sets of environmental rRNA sequences were obtained, one of them (1052 bp) with the newly tested primer set. These latter sequences encompass both the ITS1-5.8S-ITS2 region and the D1/D2 domain of the LSU rRNA gene, leading us to an accurate identification of ITS2. In turn, this allowed us to predict and show for the first time the ITS2 secondary structure of Ostreopsis. With 92 bp in length and a two-helix structure, the ITS2 of this genus revealed to be unique among the dinoflagellates. Both the PCR approach as the phylogenetic analyses allowed to place the Ostreopsis cells observed in the samples within the O. cf. ovata phylospecies’ complex, discarding the presence of O. cf. siamensis. The (phylo)genetic results point out a certain level of nucleotide sequence divergence, but were inconclusive in relation to a possible geographic origin of the O. cf. ovata population from the Algarve’s bloom. Full article
(This article belongs to the Section Marine and Freshwater Toxins)
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Open AccessArticle Transcriptional Responses of Glutathione Transferase Genes in Ruditapes philippinarum Exposed to Microcystin-LR
Int. J. Mol. Sci. 2015, 16(4), 8397-8414; doi:10.3390/ijms16048397
Received: 3 February 2015 / Revised: 20 March 2015 / Accepted: 3 April 2015 / Published: 15 April 2015
Cited by 3 | Viewed by 1062 | PDF Full-text (911 KB) | HTML Full-text | XML Full-text
Abstract
Glutathione Transferases (GSTs) are phase II detoxification enzymes known to be involved in the molecular response against microcystins (MCs) induced toxicity. However, the individual role of the several GST isoforms in the MC detoxification process is still unknown. In this study, the time-dependent
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Glutathione Transferases (GSTs) are phase II detoxification enzymes known to be involved in the molecular response against microcystins (MCs) induced toxicity. However, the individual role of the several GST isoforms in the MC detoxification process is still unknown. In this study, the time-dependent changes on gene expression of several GST isoforms (pi, mu, sigma 1, sigma 2) in parallel with enzymatic activity of total GST were investigated in gills and hepatopancreas of the bivalve Ruditapes philippinarum exposed to pure MC-LR (10 and 100 µg/L). No significant changes in GST enzyme activities were found on both organs. In contrast, MC-LR affected the transcriptional activities of these detoxification enzymes both in gills and hepatopancreas. GST transcriptional changes in gills promoted by MC-LR were characterized by an early (12 h) induction of mu and sigma 1 transcripts. On the other hand, the GST transcriptional changes in hepatopancreas were characterized by a later induction (48 h) of mu transcript, but also by an early inhibition (6 h) of the four transcripts. The different transcription patterns obtained for the tested GST isoforms in this study highlight the potential divergent physiological roles played by these isoenzymes during the detoxification of MC-LR. Full article
(This article belongs to the Section Molecular Toxicology)
Open AccessArticle Dynamics of Protein Phosphatase Gene Expression in Corbicula fluminea Exposed to Microcystin-LR and to Toxic Microcystis aeruginosa Cells
Int. J. Mol. Sci. 2011, 12(12), 9172-9188; doi:10.3390/ijms12129172
Received: 1 August 2011 / Revised: 21 November 2011 / Accepted: 30 November 2011 / Published: 8 December 2011
Cited by 9 | Viewed by 2717 | PDF Full-text (316 KB) | HTML Full-text | XML Full-text
Abstract
This study investigated the in vivo effects of microcystins on gene expression of several phosphoprotein phosphatases (PPP) in the freshwater clam Corbicula fluminea with two different exposure scenarios. Clams were exposed for 96 h to 5 µg L−1 of dissolved microcystin-LR and
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This study investigated the in vivo effects of microcystins on gene expression of several phosphoprotein phosphatases (PPP) in the freshwater clam Corbicula fluminea with two different exposure scenarios. Clams were exposed for 96 h to 5 µg L−1 of dissolved microcystin-LR and the relative changes of gene expression of three different types of PPP (PPP1, 2 and 4) were analyzed by quantitative real-time PCR. The results showed a significant induction of PPP2 gene expression in the visceral mass. In contrast, the cyanotoxin did not cause any significant changes on PPP1 and PPP4 gene expression. Based on these results, we studied alterations in transcriptional patterns in parallel with enzymatic activity of C. fluminea for PPP2, induced by a Microcystis aeruginosa toxic strain (1 × 105 cells cm−3) during 96 h. The relative changes of gene expression and enzyme activity in visceral mass were analyzed by quantitative real-time PCR and colorimetric assays respectively. The clams exhibited a significant reduction of PPP2 activity with a concomitant enhancement of gene expression. Considering all the results we can conclude that the exposure to an ecologically relevant concentration of pure or intracellular microcystins (-LR) promoted an in vivo effect on PPP2 gene expression in C. fluminea. Full article
(This article belongs to the Section Molecular Toxicology)

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