A 7-bp insertion in the 3' untranslated region suggests the duplication and concerted evolution of the rabbit SRY gene

In this work we report the genetic polymorphism of a 7-bp insertion in the 3' untranslated region of the rabbit SRY gene. The polymorphic GAATTAA motif was found exclusively in one of the two divergent rabbit Y-chromosomal lineages, suggesting that its origin is more recent than the separation of the O. c. algirus and O. c. cuniculus Y-chromosomes. In addition, the remarkable observation of haplotypes exhibiting 0, 1 and 2 7-bp inserts in essentially all algirus populations suggests that the rabbit SRY gene is duplicated and evolving under concerted evolution

Some perspective on Molecular Ecology perspectives: Are women being left out?

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/149698/1/mec15063_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/149698/2/mec15063.pd

Some perspective on Molecular Ecology perspectives: Are women being left out?

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/149698/1/mec15063_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/149698/2/mec15063.pd

Synthesis of a novel series of Cu(I) complexes bearing alkylated 1,3,5-triaza-7-phosphaadamantane as homogeneous and carbon-supported catalysts for the synthesis of 1-and 2-substituted-1,2,3-triazoles

Funding Information: This research was funded by the Funda??o para a Ci?ncia e a Tecnologia (FCT), Portugal, project UIDB/00100/2020 of the Centro de Qu?mica Estrutural, FCT/MCTES (UIDB/50006/2020 and UIDP/50006/2020) from Associate Laboratory for Green Chemistry?LAQV, Scientific Employment Stimulus?Institutional Call (CEECINST/00102/2018) and by the RUDN University Strategic Academic Leadership Program. I.L.L. acknowledges the FCT through the CATSUS PhD Program (PD/BD 135555/2018). A.G.M. was funded by Instituto Superior T?cnico, Portugal through the project CO2usE-1801P.00867.1.01 (contract no. IST-ID/263/2019). Funding Information: Funding: This research was funded by the Fundação para a Ciência e a Tecnologia (FCT), Portugal, project UIDB/00100/2020 of the Centro de Química Estrutural, FCT/MCTES (UIDB/50006/2020 and UIDP/50006/2020) from Associate Laboratory for Green Chemistry—LAQV, Scientific Employment Stimulus—Institutional Call (CEECINST/00102/2018) and by the RUDN University Strategic Academic Leadership Program. I.L.L. acknowledges the FCT through the CATSUS PhD Program (PD/BD 135555/2018). A.G.M. was funded by Instituto Superior Técnico, Portugal through the project CO2usE-1801P.00867.1.01 (contract no. IST-ID/263/2019). Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.The N-alkylation of 1,3,5-triaza-7-phosphaadamantane (PTA) with ortho-, meta-and para-substituted nitrobenzyl bromide under mild conditions afforded three hydrophilic PTA ammonium salts, which were used to obtain a new set of seven water-soluble copper(I) complexes. The new compounds were fully characterized and their catalytic activity was investigated for the low power microwave assisted one-pot azide–alkyne cycloaddition reaction in homogeneous aqueous medium to obtain disubstituted 1,2,3-triazoles. The most active catalysts were immobilized on activated carbon (AC), multi-walled carbon nanotubes (CNT), as well as surface functionalized AC and CNT, with the most efficient support being the CNT treated with nitric acid and NaOH. In the presence of the immobilized catalyst, several 1,4-disubstituted-1,2,3-triazoles were obtained from the reaction of terminal alkynes, organic halides and sodium azide in moderate yields up to 80%. Furthermore, the catalyzed reaction of terminal alkynes, formaldehyde and sodium azide afforded 2-hydroxymethyl-2H-1,2,3-triazoles in high yields up to 99%. The immobilized catalyst can be recovered and recycled through simple workup steps and reused up to five consecutive cycles without a marked loss in activity. The described catalytic systems proceed with a broad substrate scope, under microwave irradiation in aqueous medium and according to “click rules”.publishersversionpublishe

The catalytic activity of carbon-supported Cu(I)-phosphine complexes for the microwave-assisted synthesis of 1,2,3-triazoles

This research was funded by Fundação para a Ciência e a Tecnologia (FCT), Portugal, through project UIDB/00100/2020 of the Centro de Química Estrutural. It was also funded by national funds though FCT, under the Scientific Employment Stimulus-Institutional Call (CEECINST/ 00102/2018). We also acknowledge the Associate Laboratory for Green Chemistry—LAQV financed by national funds from FCT/MCTES (UIDB/50006/2020 and UIDP/50006/2020). I.L.L. is grateful to the CATSUS Ph.D. Program for her grant (PD/BD 135555/2018). AGM is grateful to Instituto Superior Técnico, Portugal for his post-doctoral fellowship through the project CO2usE-1801P.00867.1.01 (Contract No. IST-ID/263/2019). It was also supported by the RUDN University Strategic Academic Leadership Program.A set of Cu(I) complexes with 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo-[3.3.1]nonane (DAPTA) phosphine ligands viz. [CuX(κP-DAPTA)3] (1: X = Br; 2: X = I) and [Cu(µ-X)((κP-DAPTA)2]2 (3: X = Br; 4: X = I) were immobilized on activated carbon (AC) and multi-walled carbon nanotubes (CNT), as well as on these materials after surface functionalization. The immobilized copper(I) complexes have shown favorable catalytic activity for the one-pot, microwave-assisted synthesis of 1,2,3-triazoles via the azide-alkyne cycloaddition reaction (CuAAC). The heterogenized systems with a copper loading of only 1.5-1.6% (w/w relative to carbon), established quantitative conversions after 15 min, at 80 °C, using 0.5 mol% of catalyst loading (relative to benzyl bromide). The most efficient supports concerning heterogenization were CNT treated with nitric acid and NaOH, and involving complexes 2 and 4 (in the same order, 2_CNT-ox-Na and 4_CNT-ox-Na). The immobilized catalysts can be recovered and recycled by simple workup and reused up to four consecutive cycles although with loss of activity.publishersversionpublishe

PETROGRAFIA, GEOQUÍMICA E GEOCRONOLOGIA DAS ROCHAS GRANÍTICAS DA OROGENIA SAN IGNÁCIO (BOLÍVIA): Geology, geochemistry and geocronology of the granitic rocks of San Ignácio Orogeny (BOLÍVIA)

This contribution aims to characterize the Proterozoic granites of San Ignacio orogeny, western Bolivia, describing their chemical composition, U-Pb and Sm/Nd isotopic to identify sources and process of the crustal formation. The results of chemical and isotopic granitoids of Cachuela, Motacusal and Talcoso, present U/Pb age in zircon between 1307 and 1333 Ma, suggesting an important epoch of generation of granitoids in the Bolivian pre-Cambrian. Chemistry (A-Type granites) and Nd isotopes (εNd(1330) between -0.77 and -3.86) signatures here reported suggest an anorogenic environment and the spider diagram indicate the within-plates tectonic setting for the formation of these granites, instead of arc-related environment is suggested in the literature for these rocks. The data here reported suggest a geological evolution for the Bolivian pre-Cambrian composed of the San Ignacio event is represented by magmatic arc with participation of continental crust previously formed representing an important collisional period in the SW Amazonian craton.Esta contribuição visa caracterizar os granitos do Proterozóico de San Ignacio orogenia, ocidental da Bolívia, descrevendo sua composição química e isótopos de U-Pb e Sm / Nd para identificar fontes e processos de formação desyas rochas. Os resultados de granitoides químicos e isotópicos de Cachuela, Motacusal e Talcoso, apresentam idade U / Pb em zircão entre 1307 e 1333 Ma, sugerindo uma época importante de geração de granitoides no pré-Cambriano boliviano. Química (granitos de tipo A) e isótopos de Nd (εNd (1330) entre -0,77 e -3,86) aqui relatados para o pré-Cambriano boliviano indica que o evento San Ignacio, é representado por um arco magmático com participação de crosta continental previamente formada, representando um importante período colional no craton Amazônico da Amazônia

Sr ISOTOPES BY LA-MC-ICP-MS PROCEDURES COUPLED WITH THE MACS3 REFERENCE MATERIAL IN A CORAL SAMPLE: A RECORD OF ENVIRONMENTAL CHANGES: Isótopos de Sr analisados por LA-MC-ICP-MS como material de referência MACS3 em uma amostra de coral: um registro de mudanças ambientais

The main aim of this work is to demonstrate that the Laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) is a powerful tool for the analysis of strontium (Sr) isotopes in corals. This work discusses certification strategies for Sr isotopes determination, using reference material (RM) analyses and the results treatment based on detailed data acquired in biological materials, a coral sample. To obtain reliable results, it is essential to properly adjust the mass spectrometer and laser ablation system. Adjusting the equipment to its maximum intensity does not always result in correct 87Sr/86Sr ratios. Therefore, the optimization of the mass spectrometer was performed using the reference material NIST SRM-987 (solution) and adjusting the correct Sr isotope ratio to the reference material (USGS MACS3 and NIST-612, solids) before each analytical session. The protocol applied the solid reference material USGS MACS3 with an isotopic ratio 87Sr/86Sr of 0.72000. The values obtained for this RM varied between 0.7012 and 0.7014, with a correction factor calculated between 0.990 and 0.988. In order to account for potential drifts in the mass spectrometer during an analytical session, the application of bracketing correction and the use of the most convenient reference material are suggested. The analytical uncertainty of Sr data obtained by LA-MC-ICP-MS is comparable to studies carried out on other carbonate materials. The results of ablation techniques are reproducible within the analytical error, which implies that this technique produces robust results when applied to coral carbonates. In addition, several comparative measurements of different reference materials (e.g. USGS MACS3 and NIST 612) and the comparison of the 87Sr/86Sr ratios highlight the robustness of the method. The results along the coral growth axes showed a decrease in the 87Sr/86Sr ratio from the inner to the outer layer of the coral (from 0.70920 to 0.70627), which indicate variations in the availability of particulate matter during the coral growth, probably related to local marine environmental changes.- O objetivo principal deste trabalho é demonstrar que a espectrometria de massa com plasma indutivamente acoplado e ablação a laser (LA-MC-ICP-MS) é uma ferramenta poderosa para a análise de isótopos de Sr em corais. Este trabalho discute estratégias de certificação para determinação de isótopos de Sr, usando análises de material de referência e o detalhamento do tratamento dos resultados adquiridos em materiais biológicos (coral). Para obter resultados confiáveis, é essencial ajustar adequadamente o espectrômetro de massas e o sistema de ablação a laser de forma a obter a intensidade máxima e em seguida promover as correções para obter as razões 87Sr / 86Sr corretas. Nestes termos, a otimização do espectrômetro de massa foi realizada usando o material de referência NIST SRM-987 (em solução) que em sequência foi migrado para a ablação a laser com ajuste da razão isotópica Sr correta para o material de referência (NIST-612, vidro), antes de cada sessão analítica. O protocolo incluiu a utilização material de referência sólido USGS MACS3 com razão isotópica 87Sr / 86Sr de 0,72000. Os valores obtidos para esta RM variaram entre 0,7012 e 0,7014, com fator de correção calculado entre 0,990 e 0,988. A fim de contabilizar possíveis desvios no espectrômetro de massa durante uma sessão analítica, sugere-se a aplicação de correção de bracketing e o uso do material de referência com a mesma matriz. Os resultados das técnicas de ablação são reproduzíveis dentro do erro analítico, o que indica que esta técnica produz resultados robustos quando aplicada a carbonatos de coral. Além disso, várias medições comparativas de diferentes materiais de referência (por exemplo, USGS MACS3 e NIST 612) e a comparação das suas respectivas razões 87Sr / 86Sr destacam a robustez do método. Os resultados ao longo dos eixos de crescimento do coral mostraram uma diminuição na razão 87Sr / 86Sr da camada interna para a externa do coral (de 0,70920 para 0,70627). Estes resultados sugerem variações na disponibilidade de material particulado durante o crescimento do coral, provavelmente relacionado a mudanças ambientais marinhas locais. Palavras-chave: Carbonato biológico. Isótopos de Sr. LA-MC-ICP-MS. Materiais de referência. Metodologia. Ambiente marinho. &nbsp

Heterogeneous gold nanoparticle-based catalysts for the synthesis of click-derived triazoles via the azide-alkyne cycloaddition reaction

PD/BD 135555/2018 IST-ID/263/2019A supported gold nanoparticle-catalyzed strategy has been utilized to promote a click chemistry reaction for the synthesis of 1,2,3-triazoles via the azide-alkyne cycloaddition (AAC) reaction. While the advent of effective non-copper catalysts (i.e., Ru, Ag, Ir) has demonstrated the catalysis of the AAC reaction, additional robust catalytic systems complementary to the copper catalyzed AAC remain in high demand. Herein, Au nanoparticles supported on Al2 O3, Fe2 O3, TiO2 and ZnO, along with gold reference catalysts (gold on carbon and gold on titania supplied by the World Gold Council) were used as catalysts for the AAC reaction. The supported Au nanoparticles with metal loadings of 0.7–1.6% (w/w relative to support) were able to selectively obtain 1,4-disubstituted-1,2,3-triazoles in moderate yields up to 79% after 15 min, under microwave irradiation at 150◦ C using a 0.5–1.0 mol% catalyst loading through a one-pot three-component (terminal alkyne, organohalide and sodium azide) procedure according to the “click” rules. Among the supported Au catalysts, Au/TiO2 gave the best results.publishersversionpublishe