Gustavo Souza

Phylogenetic impoverishment of plant communities following chronic human disturbances in the Brazilian Caatinga.

Chronic disturbances, such as selective logging, firewood extraction and extensive grazing, may lead to the taxonomic and phylogenetic impoverishment of remaining old-growth forest communities worldwide; however, the empirical evidence on this topic is limited. We tested this hypothesis in the Caatinga vegetation--a seasonally dry tropical forest restricted to northeast Brazil. We sampled 11,653 individuals (adults, saplings, and seedlings) from 51 species in 29 plots distributed along a gradient of chronic disturbance. The gradient was assessed using a chronic disturbance index (CDI) based on five recognized indicators of chronic disturbances: proximity to urban center, houses and roads and the density of both people and livestock. We used linear models to test if mean effective number of lineages, mean phylogenetic distance and phylogenetic dispersion decreased with CDI and if such relationships differed among ontogenetic stages. As expected, the mean effective number of lineages and the mean phylogenetic distance were negatively related to CDI, and such diversity losses occurred irrespective of ontogeny. Yet the increase in phylogenetic clustering in more disturbed plots was only evident in seedlings and saplings, mostly because clades with more descendent taxa than expected by chance (e.g., Euphorbiaceae) thrived in more disturbed plots. This novel study indicates that chronic human disturbances are promoting the phylogenetic impoverishment of the irreplaceable woody flora of the Brazilian Caatinga forest. The highest impoverishment was observed in seedlings and saplings, indicating that if current chronic disturbances remain, they will result in increasingly poorer phylogenetically forests. This loss of evolutionary history will potentially limit the capacity of this ecosystem to respond to human disturbances (i.e., lower ecological resilience) and particularly their ability to adapt to rapid climatic changes in the region.

Electrochemical synthesis of TGA-capped CdTe and CdSe quantum dots

The electrochemical preparation of Te2− and Se2− ions was carried out in NaOH aqueous solution, with high yield and good stability, and applied in the preparation of negatively charged CdTe and CdSe quantum dots (QDs). A CdCl2 aqueous solution containing thioglycolic acid (TGA) stabilizer was mixed with the electrochemically generated Te2− or Se2− ions in a quite reproducible and clean one pot process, without the use of chemical reducing agents. The CdTe and CdSe QDs had good stability and high luminescence with an average size of d = 3.9 nm and 2.6 nm, respectively, the quantum yields and lifetimes were also determined. Hg2+ was efficiently quantified in the presence of the synthesized TGA-capped CdTe and CdSe, making possible the application of these QDs as chemical sensors.

In-line electrochemical reagent generation coupled to a flow injection biamperometric system for the determination of sulfite in beverage samples

This work reports an in-line electrochemical reagent generation coupled to a flow injection biamperometric procedure for the determination of SO3(2-). The method was based on a redox reaction between the I3(-) and SO3(2-) ions, after the diffusion of SO2 through a gas diffusion chamber. Under optimum experimental conditions, a linear response ranging from 1.0 to 12.0 mg L(-1) (R=0.9999 and n=7), a detection and quantification limit estimated at 0.26 and 0.86 mg L(-1), respectively, a standard deviation relative of 0.4% (n=10) for a reference solution of 4.0 mg L(-1) SO3(2-) and sampling throughput for 40 determinations per hour were achieved. Addition and recovery tests with juice and wine samples were performed resulting in a range between 92% and 110%. There were no significant differences at a 95% confidence level in the analysis of eight samples when comparing the new method with a reference procedure.

Fluorescence probe for mercury(II) based on the aqueous synthesis of CdTe quantum dots stabilized with 2-mercaptoethanesulfonate

Manipulation of the QD surface by changing morphology and surface capping ligands, as well as adjusting nanocrystal size, plays a crucial role on the selectivity and sensitivity exhibited by QDs towards a given target analyte. In this study, a novel aqueous synthesis of CdTe QDs capped with a thiol compound containing a sulfonate (SO3−) terminal group, viz., 2-mercaptoethanesulfonate (MES), was thoroughly investigated with the aim of obtaining a fluorescent probe for chemical analysis. The results obtained with the prepared CdTe-MES QDs in the determination of various metal ions demonstrated the high efficiency of these nanomaterials for determining Hg(II) levels. Upon optimization, linear working calibration curves for Hg(II) concentrations of up to 0.5 μmol L−1 were obtained, with a determination coefficient of 0.9984. The detection limit was 0.0095 μmol L−1 and the quantification limit was 0.0324 μmol L−1. When applied to the determination of Hg(II) in tap water samples, the developed method provided analytical results similar to those obtained with a reference method. The accuracy and precision of both methods were comparatively evaluated using the Students t-test and the Fischer test, and the tabulated values showed a good agreement at a 95% confidence level.

Clean photoinduced generation of free reactive oxygen species by silica films embedded with CdTe–MTA quantum dots

CdTe quantum dots capped with mercaptopropionic acid, 3.5 nm in size, were entrapped in sol–gel films prepared with tetramethyl orthosilicate under mineral acidic catalysis in the presence of Triton X-100 as a non-ionic surfactant. The follow-up of the sol–gel process was performed in real-time both with fluorescent crystal violet as a molecular rotor and with quantum dots. Clusters of nanoparticles 500 nm in size become homogeneously distributed in the films, but preserving initial photoluminescence quantum yields (21%), and the emission spectrum had increased excited state lifetimes (65 ± 4 ns) and photostability. Films photoactivation inside a multi-pumping flow system enabled reproducible generation of reactive oxygen species as determined by chemiluminescence using the alkaline luminol reagent, thus opening future developments for clean and environmentally friendly analytical applications.

Interstitial telomeric sites and Robertsonian translocations in species of Ipheion and Nothoscordum (Amaryllidaceae)

The genera Nothoscordum and Ipheion (Allioideae, Amaryllidaceae) are cytologically characterized by a dysploid series with variable numbers of metacentric and acrocentric chromosomes typical of karyotypes rearranged by Robertsonian translocations (RT). Since they have large chromosomes, low diploid numbers, and possess two telomeric motifs [the vertebrate-type (TTAGGG)n and the Arabidopsis-type (TTTAGGG)n] they are suitable for investigating the occurrence and possible role of interstitial telomeric sites (ITS) associated with RT. We analyzed the distributions of telomeric sites in 12 species of Nothoscordum and Ipheion and found that both telomeric probes colocalized in all chromosome termini. Cloning and sequencing PCR products obtained using both telomeric primers simultaneously revealed long stretches of (TTAGGG)n and (TTTAGGG)n sequences together with degenerated telomeric sequences. Most acrocentric chromosomes have a 45S rDNA site at the terminal region of the short arms adjacent to the most distal telomeric sites. Telomeric signals were found at all chromosome ends, but ITS were also detected in a few proximal and subterminal regions in some Nothoscordum species. Although RT are common in this group of plants, our findings suggest that proximal positioning of telomeric motifs are not necessarily related to that kind of rearrangement. Rather, transposition of telomeric sequences followed by amplification, could better explain the presence of (TTAGGG)n and (TTTAGGG)n repeats at those sites. Furthermore, a few small interstitial sites found in some Nothoscordum species indicate that dispersion of these sequences was not restricted to the proximal region.

Employment of electrochemically synthesized TGA-CdSe quantum dots for Cr(3+) determination in vitamin supplements.

The fluorescence quenching of TGA-CdSe quantum dots (QDs) was used for Cr(3+) quantification in vitamin supplements. The QD was electrochemically synthesized, demonstrating high reproducibility with control of particle size, thus making it a clean method, without the presence of reducing agents. Under ideal conditions, with the fluorescence band at 551 nm (excitation 365 nm), the maximum fluorescence quenching was observed at pH 4.0, with a time of 200 s for each data acquisition. Under optimum experimental conditions, linear quenching was observed for Cr(3+) in the range of 25.0-325.0 ng L(-1) (R=0.9996, n=6), a limit of detection of 5.67 ng L(-1), and relative standard deviation of 4.43% (n=10). The recovery test for Cr(3+) quantification in vitamin supplements presented results from 82% to 98%. These Cr(3+) determination results were compared to the same vitamin supplement sample using flame atomic absortion spectrometry (FAAS) method, and no significant differences were observed at 95% confidence level.