22 research outputs found

    Novedades corológicas para la flora vascular de la sierra de Gredos (Sistema Central, España)

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    In the present paper, 58 chorological novelties for Gredos range (Central System, Spain) are showed. Some of them represent important disjunctions with respect to known Iberian distribution, as the cases of Cytinus ruber (Fourr.) Fritsh, Isolepis fluitans (L.) R.Br., Alyssum montanum L. and Lysimachia ephemerum L. Some species, such as Carex lainzii Luceño, E. Rico & T. Romero, Iberodes brassicifolia (Lag.) Serrano, R. Carbajal & S. Ortiz, Lycopodiella inundata (L.) J. Holub and Tephroseris coincyi (Rouy) Holub are of great interest from a conservational point of view. Finally, we present a number of provincial novelties, mainly for Ávil

    Procurement and characterization of cellulose nanocrystals from cassava bagasse (Manihot esculenta Crantz)

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    ABSTRACT Objective: Obtaining and characterizing cellulose nanocrystals from cassava bagasse. Design/methodology/approach: Cellulose nanocrystals were obtained from cassava bagasse by acid hydrolysis (HCI), ultrasonication, centrifugation, dialysis, deep freezing and lyophilization. The cassava bagasse and the cellulose nanocrystals obtained were physiochemically characterized by Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD) and Scanning Electron Microscopy with Coupled Elemental Analysis (SEM-EDS). As an additional technique, Atomic Force Microscopy (AFM) was used. Results: The analyzes performed show that the cellulose obtained was type Iβ. This study reports a percentage of crystallinity of cassava bagasse cellulose of 37.1%, increasing the percentage to 48% of crystallinity in cellulose nanocrystals. The diameters of the cassava bagasse fibers were reported to be 2 μm and their elemental composition (SEM-EDS) mainly constituted by carbon (C), oxygen (O) and traces of (N). The morphology observed through AFM of the nanocrystals of cassava bagasse (Manihot esculenta) was rod-shaped, with a helical appearance without residual charge, with diameters between 8.7 and 9.3 nm. Limitations on study/implications: The acid hydrolysis process showed a low percentage of crystallinity, although higher than other works reported for cassava bagasse. Findings/conclusions: The results obtained show the possibility of obtaining cellulose nanocrystals from cassava bagasse ().    Objective: To procure and characterize cellulose nanocrystals from cassava bagasse. Design/methodology/approach: Cellulose nanocrystals were obtained from cassava bagasse by acid hydrolysis (HCI), ultrasonication, centrifugation, dialysis, deep freezing and lyophilization. The cassava bagasse and the cellulose nanocrystals obtained were physicochemically characterized by Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD) and Scanning Electron Microscopy with Coupled Elemental Analysis (SEM-EDS). As an additional technique, Atomic Force Microscopy (AFM) was used. Results: The analyses performed show that the cellulose obtained was type Iβ. This study reports a percentage of crystallinity of the cassava bagasse cellulose of 37.1%, increasing the percentage to 48% crystallinity in cellulose nanocrystals. The diameters of the cassava bagasse fibers were reported to be 2 μm and their elemental composition (SEM-EDS) mainly constituted by carbon (C), oxygen (O) and traces of nitrogen (N). The morphology observed through AFM of the nanocrystals of cassava bagasse (Manihot esculenta) was rod-shaped, with helicoidal appearance without residual charge, with diameters between 8.7 and 9.3 nm. Limitations on study/implications: The acid hydrolysis process showed a low percentage of crystallinity, although higher than other works reported for cassava bagasse. Findings/conclusions: The results obtained confirm the possibility of obtaining cellulose nanocrystals from cassava bagasse (Manihot esculenta)

    Novedades corológicas y nomenclaturales para la flora vascular de la Sierra de Gredos (Sistema Central), III

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    In the present paper we present the floristic novelties for the flora of the Sierra de Gredos resulting from the explorations of these mountains and that, mostly, are the result of the field trips of the year 2021. We present 31 chorological novelties, among which we highlight the finding in the Community of Madrid of the restricted endemic Iberodes brassicifolia (Lag.) M. Serrano, R. Carbajal & S. Ortiz. Also relevant are Herniaria hirsuta L., Rosa glauca Pourr. (new for the Spanish Central System) and Rosa coriifolia Fr. (new for Extremadura and the whole of the Sierra de Gredos), as well as Soliva sessilisRuiz & Pav., Trifolium vesiculosumSavi (new for Castilla y León) and Lepidium villarsii Gren. & Godr. subsp. villarsii (new for the Sierra de Gredos). Finally, two new nomenclatural combinations are made in the genus Tephroseris (Rchb.) Rchb.: Tephroseris balbisiana (DC.) Holub subsp. coincy (Rouy) P. Vargas & Luceño, endemic to Gredos range, and Tephroseris balbisiana subsp. elodes (Boiss. ex DC.) P. Vargas & Luceño, endemic to Sierra Nevada

    Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

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    Background: Severe spermatogenic failure (SPGF) represents one of the most relevant causes of male infertility. This pathological condition can lead to extreme abnormalities in the seminal sperm count, such as severe oligozoospermia (SO) or non-obstructive azoospermia (NOA). Most cases of SPGF have an unknown aetiology, and it is known that this idiopathic form of male infertility represents a complex condition. In this study, we aimed to evaluate whether common genetic variation in TEX15, which encodes a key player in spermatogenesis, is involved in the susceptibility to idiopathic SPGF.Materials and Methods: We designed a genetic association study comprising a total of 727 SPGF cases (including 527 NOA and 200 SO) and 1,058 unaffected men from the Iberian Peninsula. Following a tagging strategy, three tag single-nucleotide polymorphisms (SNPs) of TEX15 (rs1362912, rs323342, and rs323346) were selected for genotyping using TaqMan probes. Case-control association tests were then performed by logistic regression models. In silico analyses were also carried out to shed light into the putative functional implications of the studied variants.Results: A significant increase in TEX15-rs1362912 minor allele frequency (MAF) was observed in the group of SO patients (MAF = 0.0842) compared to either the control cohort (MAF = 0.0468, OR = 1.90, p = 7.47E-03) or the NOA group (MAF = 0.0472, OR = 1.83, p = 1.23E-02). The genotype distribution of the SO population was also different from those of both control (p = 1.14E-02) and NOA groups (p = 4.33-02). The analysis of functional annotations of the human genome suggested that the effect of the SO-associated TEX15 variants is likely exerted by alteration of the binding affinity of crucial transcription factors for spermatogenesis.Conclusion: Our results suggest that common variation in TEX15 is involved in the genetic predisposition to SO, thus supporting the notion of idiopathic SPGF as a complex trait

    Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

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    Lisbon clinical group co-authors and IVIRMA group co-authors Ana Aguiar, (Unidade de Medicina da Reproducao, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal); Carlos Calhaz-Jorge, (Unidade de Medicina da Reproducao, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal); Joaquim Nunes, (Unidade de Medicina da Reproducao, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal); Sandra Sousa (Unidade de Medicina da Reproducao, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal), and Sónia Correia (Centro de Medicina Reprodutiva, Maternidade Alfredo da Costa, Centro Hospitalar Lisboa Central, Lisboa, Portugal); Maria Graça Pinto(Centro de Medicina Reprodutiva, Maternidade Alfredo da Costa, Centro Hospitalar Lisboa Central, Lisboa, Portugal). Alberto Pacheco, (IVIRMA Madrid, Spain); Cristina González, (IVIRMA Sevilla, Spain); Susana Gómez, (IVIRMA Lisboa, Portugal); David Amorós, (IVIRMA Barcelona, Spain); Jesús Aguilar, (IVIRMA Vigo, Spain); Fernando Quintana, (IVIRMA Bilbao, Spain).Background: Severe spermatogenic failure (SPGF) represents one of the most relevant causes of male infertility. This pathological condition can lead to extreme abnormalities in the seminal sperm count, such as severe oligozoospermia (SO) or non-obstructive azoospermia (NOA). Most cases of SPGF have an unknown aetiology, and it is known that this idiopathic form of male infertility represents a complex condition. In this study, we aimed to evaluate whether common genetic variation in TEX15, which encodes a key player in spermatogenesis, is involved in the susceptibility to idiopathic SPGF. Materials and Methods: We designed a genetic association study comprising a total of 727 SPGF cases (including 527 NOA and 200 SO) and 1,058 unaffected men from the Iberian Peninsula. Following a tagging strategy, three tag single-nucleotide polymorphisms (SNPs) of TEX15 (rs1362912, rs323342, and rs323346) were selected for genotyping using TaqMan probes. Case-control association tests were then performed by logistic regression models. In silico analyses were also carried out to shed light into the putative functional implications of the studied variants. Results: A significant increase in TEX15-rs1362912 minor allele frequency (MAF) was observed in the group of SO patients (MAF = 0.0842) compared to either the control cohort (MAF = 0.0468, OR = 1.90, p = 7.47E-03) or the NOA group (MAF = 0.0472, OR = 1.83, p = 1.23E-02). The genotype distribution of the SO population was also different from those of both control (p = 1.14E-02) and NOA groups (p = 4.33–02). The analysis of functional annotations of the human genome suggested that the effect of the SO-associated TEX15 variants is likely exerted by alteration of the binding affinity of crucial transcription factors for spermatogenesis. Conclusion: Our results suggest that common variation in TEX15 is involved in the genetic predisposition to SO, thus supporting the notion of idiopathic SPGF as a complex trait.This work was supported by the Spanish Ministry of Science and Innovation through the Spanish National Plan for Scientific and Technical Research and Innovation (PID 2020-120157RB-I00) and the Andalusian Government through the research projects of “Plan Andaluz de Investigacion, Desarrollo e Innovacion (PAIDI 2020)” (ref. PY20_00212) and “Programa Operativo FEDER 2020” (ref. B-CTS-584-UGR20). LB-C was supported by the Spanish Ministry of Science and Innovation through the “Juan de la Cierva Incorporacion” program (Grant ref. IJC 2018-038026- I, funded by MCIN/AEI/10.13039/501100011033), which includes FEDER funds. AG-J was funded by MCIN/AEI/ 10.13039/501100011033 and FSE “El FSE invierte en tu futuro” (grant ref. FPU20/02926). IPATIMUP integrates the i3S Research Unit, which is partially supported by the Portuguese Foundation for Science and Technology (FCT), financed by the European Social Funds (COMPETE-FEDER) and National Funds (projects PEstC/SAU/LA0003/2013 and POCI-01-0145-FEDER-007274). PM is supported by the FCT post-doctoral fellowship (SFRH/BPD/120777/2016), financed from the Portuguese State Budget of the Ministry for Science, Technology and High Education and from the European Social Fund, available through the Programa Operacional do Capital Humano. ToxOmics—Centre for Toxicogenomics and Human Health, Genetics, Oncology and Human Toxicology, Nova Medical School, Lisbon, is also partially supported by FCT (UID/BIM/00009/2016 and UIDB/00009/2020). SL received support from Instituto de Salud Carlos III (grant: DTS18/00101], co-funded by FEDER funds/European Regional Development Fund (ERDF)-a way to build Europe-), and from “Generalitat de Catalunya” (grant 2017SGR191). SL is sponsored by the “Researchers Consolidation Program” from the SNS-Dpt. Salut Generalitat de Catalunya (Exp. CES09/020). This article is related to the Ph.D. Doctoral Thesis of AG-J.info:eu-repo/semantics/publishedVersio

    Evidence of spatial clustering of childhood acute lymphoblastic leukemia cases in Greater Mexico City: report from the Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia

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    BackgroundA heterogeneous geographic distribution of childhood acute lymphoblastic leukemia (ALL) cases has been described, possibly, related to the presence of different environmental factors. The aim of the present study was to explore the geographical distribution of childhood ALL cases in Greater Mexico City (GMC).MethodsA population-based case-control study was conducted. Children <18 years old, newly diagnosed with ALL and residents of GMC were included. Controls were patients without leukemia recruited from second-level public hospitals, frequency-matched by sex, age, and health institution with the cases. The residence address where the patients lived during the last year before diagnosis (cases) or the interview (controls) was used for geolocation. Kulldorff’s spatial scan statistic was used to detect spatial clusters (SCs). Relative risks (RR), associated p-value and number of cases included for each cluster were obtained.ResultsA total of 1054 cases with ALL were analyzed. Of these, 408 (38.7%) were distributed across eight SCs detected. A relative risk of 1.61 (p<0.0001) was observed for the main cluster. Similar results were noted for the remaining seven ones. Additionally, a proximity between SCs, electrical installations and petrochemical facilities was observed.ConclusionsThe identification of SCs in certain regions of GMC suggest the possible role of environmental factors in the etiology of childhood ALL

    Lupinus bicolor Lindl. (Fabaceae), a new species for the Palearctic vascular flora

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    En el presente artículo damos a conocer por primera vez la presencia en el Viejo Mundo de Lupinus bicolor Lindl., una planta nativa del SO de Norteamérica. Las poblaciones han sido halladas en la sierra de Gredos, donde crecen principalmente en prados primaverales temporalmente inundados del dominio de Quercus pyrenaica Willd. Tras un estudio morfológico, no hemos encontrado ninguna diferencia entre las poblaciones gredenses y las del continente americano. La presencia de L. bicolor en la península ibérica es probablemente el resultado de una introducción humana, si bien son necesarios estudios más profundos para descartar completamente el origen natural de estas poblaciones

    An integrative monograph of Carex section Schoenoxiphium (Cyperaceae)

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    Carex section Schoenoxiphium (Cariceae, Cyperaceae) is endemic to the Afrotropical biogeographic region and is mainly distributed in southern and eastern Africa, with its center of diversity in eastern South Africa. The taxon was formerly recognized as a distinct genus and has a long history of taxonomic controversy. It has also an important morphological and molecular background in particular dealing with the complexity of its inflorescence and the phylogenetic relationships of its species. We here present a fully updated and integrative monograph of Carex section Schoenoxiphium based on morphological, molecular and cytogenetic data. A total of 1,017 herbarium specimens were examined and the majority of the species were studied in the field. Previous molecular phylogenies based on Sanger-sequencing of four nuclear and plastid DNA regions and RAD-seq were expanded. For the first time, chromosome numbers were obtained, with cytogenetic counts on 44 populations from 15 species and one hybrid. Our taxonomic treatment recognizes 21 species, one of them herein newly described (C. gordon-grayae). Our results agree with previous molecular works that have found five main lineages in Schoenoxiphium. We provide detailed morphological descriptions, distribution maps and analytical drawings of all accepted species in section Schoenoxiphium, an identification key, and a thorough nomenclatural survey including 19 new typifications and one nomen novum

    Novelties of the Sierra de Gredos bryoflora (Central System, Spain), with special remarks on the autonomous community of Extremadura

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    En este artículo se presentan numerosas novedades corológicas de interés, basadas en las colectas llevadas a cabo durante los años 2016 y 2017 en los pisos oro y crioromediteráneo de la sierra de Gredos, zonas que habían sido escasamente colectadas. Entre los resultados destacamos el hallazgo de Douinia ovata, desconocida de la región mediterránea española, y de Sciurohypnum reflexum y Tortula hoppeana, nuevos para el Sistema Central en su conjunto. Destacamos también 4 hepáticas y 24 musgos nuevos para la Comunidad Autónoma de Extremadura, así como otras no conocidas para la sierra de Gredos o las provincias de Ávila o Salamanca. Por último, se incluyen citas de nuevas poblaciones de briófitos muy raros en Gredos o el Sistema Central en su conjunt

    Confirmation of Carex pseudobrizoides Clavaud (Cyperaceae) in the Iberian Peninsula and other contributions to the knowledge of the iberian Carex

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    This article shows some contributions to the knowledge of the genus Carex (Cyperaceae) in the Iberian Peninsula. Among them we highlight the confirmation of C. pseudobrizoides Clavaud for the Iberian Peninsula (Basque Country). The results of the morphological study carried out to differentiate this species from the closely related C. brizoides L., also present in the territory, are showed. A map of the Iberian distribution of C. praecox Schreb. is provided. C. umbrosa is cited for the first time for the Iberian System, the presence of C. montana L. in this mountain system is rejected, the distribution area of C. riparia in Eastern Andalusia is discussed, and a new chromosome number for C. olbiensis Jord. is reporte
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