Symmetrical Observability of Kinematic Parameters in Symmetrical Parallel Mechanisms

This article presents an application of symmetry group theory in kinematic identification of parallel mechanisms of nlegs legs -- Kinematic Identification implies the estimation of the actual geometrical parameters (as opposed to nominal ones) of a physical mechanism -- For a symmetric mechanism, KI requires configuring sets of leg positions with symmetrical observability – This article presents as main contributions: (i) a conjecture that allows mapping the symmetries of the mechanism into the active-joint workspace, (ii) a set of necessary conditions to express leg parameters in coordinate systems which allow symmetrical observability, and (iii) a procedure for exploiting symmetries in pose selection for kinematic identification of symmetrical parallel mechanisms -- For the kinematic identification itself, we adopt a divide-and-conquer (DC) identification protocol -discussed by us in another publication- in which each leg of the mechanism is independently identified by using the inverse calibration method -- In this article we emphasize how to exploit the symmetries existent in (nlegs − 1) legs of the parallel mechanism allowing to apply to other legs the symmetry-transformed sample protocol used for the kinematic identification of a reference leg -- The symmetrical observability of sets of leg parameters allows to reduce the costs of the pose selection procedure by a factor of (1/nlegs) compared to a complete DC procedure in which the poses of each leg are selected independently -- The pose selection is carried out only for the reference leg -- For the (nlegs−1) remaining legs the poses are dictated by symmetry operations performed onto the poses of the reference leg -- An application of the symmetrical observability is presented through the simulated kinematic identification of a 3RRR symmetrical parallel mechanismPolytechnic School of the University of São PauloSitio webIndicaciones, Associação Brasileira de Métodos Computacionais em Engenharia, International Association for Computational Mechanics, International Congress and Convention Association, Conheça o São Paulo é Tudo de Bom, Embratur, PETROBRA

Molecular dynamics simulation of the nanoindentation process in Cr/CrN and (Cr/CrN)2 thin films

Molecular dynamics (MD) simulations were carries out for studying the influenceof nanoindentation in the atomistic deformation mechanisms of Cr/CrN and(Cr/CrN)2 coatings with BCC and FCC crystalline structures for Cr and CrN,respectively. The Morse potential was employed in order to determine the atomicinteraction forces of the Cr-Cr and Cr-N atoms. A non-deformable potential solidsphere was implemented for determining the role of the nanoindenter. The OliverParr method (OP) was used to obtain the hardness and elastic modulus of the Cr/CrN and (Cr/CrN)2 layers, resulting in values of 18 and 20 GPa for Cr/CrN and (Cr/CrN)2, respectively. The Cheng method was used for correcting the hardness values obtained by the OP method. The Cheng correction showed higher hardness values since it avoids the influence of the scale effect. Regarding the elasticity modulus, Cr/CrN and (Cr/CrN)2 exhibited values of 217.86 GPa and 258.9 GPa, respectively. Simulations of the temperature influence on the hardness were carried out over a range of 300-1000 K. Results indicate that the hardness decreased as a function of the temperature.Fil: Amaya Roncancio, Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Física Aplicada "Dr. Jorge Andrés Zgrablich". Universidad Nacional de San Luis. Facultad de Ciencias Físico Matemáticas y Naturales. Instituto de Física Aplicada "Dr. Jorge Andrés Zgrablich"; ArgentinaFil: Arias Mateus, D. F.. Universidad Católica de Pereira; ColombiaFil: Segura Giraldo, B.. Universidad Nacional de Colombia; ColombiaFil: de la Roche, J.. Universidad Nacional de Colombia; ColombiaFil: Restrepo Parra, E.. Universidad Nacional de Colombia; Colombi

Nuevas tendencias en el diseño de materiales y estructuras

El presente texto incluye temas como las nuevas herramientas para la modelación de diferentes problemas relacionados con la Ingeniería Civil; la implantación de un modelo matemático para el análisis dinámico no lineal de las viviendas prefabricadas, que permite simular el comportamiento histerético del sistema estructural de la vivienda a partir del comportamiento cíclico experimental; las herramientas de la inteligencia artificial (las redes neuronales) para la modelación de fenómenos complejos presentes en el comportamiento de algunos materiales, en este caso en tres arenas típicas y su relación esfuerzo-deformación; nuevos enfoques en el diseño de estructuras y materiales, nuevas tendencias de diseño tanto de las estructuras como en los materiales compuestos; una perspectiva sobre nuevos materiales compuestos o alternativos, que proponen materiales de origen natural combinados con materiales tradicionales en la industria de la construcción. Presenta una breve descripción de los materiales compuestos, tipo sándwich, y propone un nuevo compuesto a partir de conglomerados de material vegetal y ferrocemento. E incluye el estudio de los suelos residuales estabilizados con cal y se evalúa su comportamiento mecánico.PRÓLOGO............. 15 PRESENTACIÓN.............. 17 Primera parte Nuevas herramientas para la modelación de problemas en Ingeniería Civil Capítulo 1 APLICACIÓN DEL MODELO DE Bouc y Wen EN EL ANÁLISIS SÍSMICO DE VIVIENDAS PREFABRICADAS Daniel Alveiro Bedoya Ruiz 1.1 INTRODUCCIÓN.............. 21 1.2 AVANCES EN EL MODELO DE Bouc y Wen............. 23 1.3 SISTEMAS HISTERÉTICOS NO LINEALES............ 27 1.3.1 Ecuación de movimiento............ 30 1.3.2 Parámetros de forma de la histéresis............ 31 1.3.3 Disipación de energía............. 34 1.3.4 Rigidez, resistencia y estrangulamiento..............35 1.4 Identificación de sistemas y control.............. 37 1.5 APLICACIÓN DEL MODELO EN VIVIENDAS PREFABRICADAS............. 38 1.5.1 El modelo en casas prefabricadas de ferrocemento............. 41 1.5.2 Dinámica y comportamiento no lineal............. 44 1.6 CONCLUSIÓN............ 45 Capítulo 2 DETERMINACIÓN DE LA RELACIÓN CONSTITUTIVA DE LAS ARENAS USANDO REDES NEURONALES ARTI FICIALES (RNA) Hernán Eduardo Martínez-Carvajal - Márcio Muniz de Farias 2.1 INTRODUCCIÓN............ 51 2.2 MODELAMIENTO CONSTITUTIVO DE MATERIALES........... 53 2.3 MODELAMIENTO CONSTITUTIVO USANDO REDES NEURONALES ARTIFICIALES............. 55 2.4 LA BASE DE DATOS............ 56 2.5 LA ARQUITECTURA DE LA RED NEURONAL............... 58 2.6 RESULTADOS DE LA SIMULACIÓN............. 60 2.7. CONCLUSIONES.............. 65 Segunda parte Nuevos enfoques en el diseño de materiales y estructuras Capítulo 3 Diseño por desplazamientos de pilares de puentes Matthew J. Tobolski - José I. Restrepo 3.1 INTRODUCCIÓN............ 69 3.2 ESPECTRO DEL DISEÑO............. 72 3.3 AMORTIGUAMIENTO............ 74 3.4 RESPUESTA INÉLASTICA............. 75 3.5 COMBINACIÓN DE FACTORES DE AMPLIFICACIÓN DE DESPLAZAMIENTO............. 79 3.6 CAPACIDAD DE DESPLAZAMIENTO............ 80 3.7 PROCEDIMIENTO DE DISEÑO............ 85 3.8 OBJETIVO DE DESEMPEÑO DE SEGURIDAD DE LA VIDA.............. 86 3.9 OBJETIVO DE DESEMPEÑO DE FUNCIONAMIENTO INMEDIATO.............. 89 3.10 DISEÑO DE LOS ELEMENTOS............. 92 3.11 ANÁLISIS PARAMÉTRICO............. 93 3.12 EXIGENCIA SÍSMICA Y DUCTILIDAD DE CURVATURA.............. 93 3.13 PROPORCIÓN DE LA ROTACIÓN RESIDUAL............. 94 3.14 DIÁMETRO Y ALTURA DE LA COLUMNA.............. 95 3.15 CONCLUSIONES.............. 98 3.16 APÉNDICE. EJEMPLO DE DISEÑO............... 99 Capítulo 4 UN NUEVO ENFOQUE PARA EL ANÁLISIS Y DISEÑO DE ESTRUCTURAS DE HORMIGÓN ARMADO Héctor Guillermo Urrego Giraldo 4.1 INTRODUCCIÓN.............. 111 4.2 COMPORTAMIENTO DEL HORMIGÓN............. 113 4.3 COMPORTAMIENTO DEL ACERO.............. 115 4.4 CURVATURA.............. 117 4.5 EJEMPLO 1.............. 123 4.6 MÉTODO PROPUESTO............... 136 4.7 EJEMPLO 2............. 138 4.8 CONCLUSIONES............... 144 Capítulo 5 DESEMPEÑO SÍSMICO DE PÓRTI COS PLANOS DE ACERO CON EL SISTEMA KNEE-BRACING Ricardo León Bonett Díaz - Carolina López Toro 5.1 INTRODUCCIÓN.............. 147 5.2 MARCO CONCEPTUAL.............. 149 5.3 CRITERIOS PARA ESCOGER EL KNEE Y EL BRACE.............. 151 5.4 CASO DE ESTUDIO............. 153 5.5 INCORPORACIÓN DEL DISPOSABLE KNEE BRACING............. 165 5.6 EVALUACIÓN DE LA CAPACIDAD SÍSMICA............. 167 5.7 ANÁLISIS DE RESULTADOS.............. 172 5.8 CONCLUSIONES................ 176 Capítulo 6 TENDENCIAS EN EL DISEÑO DE MEZCLAS ASFÁLTI CAS EN CALIENTE ¡MARSHALL vs SUPERPAVE! Carlos Rodolfo Marín Uribe 6.1 INTRODUCCIÓN.............. 179 6.2 DESCRIPCIÓN DE LAS METODOLOGÍAS DE DISEÑO............... 180 6.3 Algunas diferencias entre las dos metodologías.............. 190 6.4 DESARROLLO DE UN TRABAJO EXPERIMENTAL.............. 192 6.4.1 Selección de materiales............ 192 6.4.2 Obtención del porcentaje óptimo de asfalto........... 195 6.4.3 Caracterización mecánica y dinámica de las mezclas asfálticas............. 195 6.5 ANÁLISIS DE RESULTADOS.............. 203 6.6 CONCLUSIONES............... 204 Capítulo 7 EL EFECTO ARCO EN SUELOS John Mario García Giraldo 7.1 INTRODUCCIÓN............. 209 7.2 EL ARCO COMO FORMA ESTRUCTURAL.............. 210 7.2.1 Definición de arco.............. 210 7.2.2 Historia del arco como elemento estructural............. 211 7.3 F ORMAS DE ARCO............ 212 7.4 EFECTO DE LA GEOMETRÍA ESTRUCTURAL EN LA DISTRIBUCIÓN DE TENSIONES EN EL INTERIOR DE UN ELEMENTO............. 215 7.4.1 Esfuerzos en un elemento estructural............. 215 7.4.2 Distribución de tensiones en el interior de un elemento estructural............. 216 7.5 GEOMETRÍAS ÓPTIMAS............... 219 7.6 ESTUDIO DEL EFECTO ARCO EN LOS SUELOS............ 220 7.6.1 Efecto de arco sobre una escotilla móvil (trapdoor).............. 220 7.6.2 Análisis del efecto arco en los suelos por Terzaghi en 1945........... 222 7.7 ANÁLISIS DEL EFECTO ARCO EN LOS SUELOS POR HANDY EN 1985.............. 226 7.8 ANÁLISIS DEL EFECTO ARCO EN LOS SUELOS POR HARROP EN 1989.............. 233 7.9 ANÁLISIS DEL EFECTO ARCO EN LOS SUELOS POR SALGADO EN 2002.............. 237 7.10 CONCLUSIONES............ 241 Tercera parte Nuevos materiales compuestos o alternativos Capítulo 8 MATERIALES COMPUESTOS A BASE DE FERROCEMENTO Y MATERIAL VEGETA L Daniel Alveiro Bedoya Ruiz - Juan Camilo Aldana Barrera - Leonardo Ávila Vélez 8.1 INTRODUCCIÓN.............. 247 8.2 MATERIALES COMPUESTOS.............. 249 8.2.1 Núcleo............. 252 8.2.2 Corteza estructural............. 253 8.2.3 Sistemas constructivos............ 254 8.3 COMPORTAMIENTO EXPERIMENTAL DE LOS COMPUESTOS DE FERROCEMENTO Y MATERIAL VEGETAL............. 255 8.3.1 Núcleo de material vegetal............ 256 8.3.2 Corteza de ferrocemento.............. 260 8.3.3 A. 3.3 paneles de ferrocemento con núcleo vegetal............. 261 8.4 CONCLUSIONES.............. 266 Capítulo 9 COMPORTAMIENTO MECÁNICO DE SUELOS RESIDUALES ESTABILIZADO S César Augusto Hidalgo Montoya - Mario Alberto Rodríguez Moreno 9.1 INTRODUCCIÓN.............. 271 9.2 ESTABILIZACIÓN DE SUELOS CON CAL............. 273 9.3 PROPIEDADES RESILIENTES O RESILIENCIA............... 275 9.4 CARGAS EN EL PAVIMENTO.............. 276 9.4.1 Tipos de cargas que actúan............. 276 9.4.2 Duración de la carga cíclica............. 279 9.5 MÓDULO RESILIENTE............. 279 9.6 F ACTORES GENERALES QUE AFECTAN EL MÓDULO RESILIENTE............. 281 9.6.1 Factores que afectan el Mr de suelos finos............ 281 9.6.2 Factores que afectan el Mr de materiales granulares............ 284 9.7 ENSAYOS PARA DETERMINAR EL MÓDULO RESILIENTE.............. 286 9.8 CORRELACIONES............... 289 9.9 PROPIEDADES RESILIENTES DE SUELOS ESTABILIZADOS.............. 290 9.10 ENSAYOS DE LABORATORIO.............. 292 9.11 ANÁLISIS DE RESULTADOS............... 295 9.11.1 Compresión simple............ 296 9.11.2 Tracción indirecta............. 299 9.11.3 CBR............. 300 9.11.4 Módulo resiliente.............. 302 9.12 CONCLUSIONES.............. 30

Estándares para registrar señales de ecolocalización y construir bibliotecas de referencia de murciélagos en Colombia

Bioacoustic tools allow monitoring bats usually not detected with traditional methods, such as mist nets, and also provide information about different biological aspects of the species. The interest in applying these methods has increased in the last years, and consequently, there has been a rapid development of ultrasonic recording equipment and analysis tools. However, in the Neotropics, bat bioacoustics is emerging in some countries and just appearing in others; therefore it is necessary to reinforce this field to study the high taxonomic and functional diversity of the region. Therefore, it is essential to have bat call libraries that serve as a reference to validate and compare recordings from different species and localities. Some countries in the Neotropics have advanced in this process and are already building these reference libraries. In Colombia, the future work is challenging, due to the more than 200 bat species present. This paper establishes the methodological basis to obtain bat-reference calls in Colombia and allow those who are just starting out in this research field.La bioacústica permite monitorear murciélagos difícilmente detectados con métodos tradicionales, como las redes de niebla, y permiten obtener información sobre diferentes aspectos de la biología de las especies de estudio. En los últimos años se ha incrementado el interés por la aplicación de estos métodos y, en consecuencia, ha sido rápido el desarrollo de los equipos de grabación ultrasónica y las herramientas de análisis. Sin embargo, en el Neotrópico la bioacústica de murciélagos está en etapa de crecimiento en algunos países y apenas ahora está apareciendo en otros, por lo cual es necesario fortalecer este campo para estudiar la alta diversidad taxonómica y funcional de la región. En este contexto, es indispensable contar con bibliotecas de señales acústicas, que sirvan como referencia para identificar, validar y comparar las grabaciones de diferentes especies y localidades. Algunos países del Neotrópico han avanzado en este proceso y están construyendo estas bibliotecas de referencia. En Colombia, el trabajo a futuro implica un reto, debido a las más de 200 especies de murciélagos presentes. Este trabajo presenta las bases metodológicas para tomar grabaciones de referencia de murciélagos en Colombia y generar una guía para aquellos que se están iniciando en este campo de investigación

Genera of phytopathogenic fungi: GOPHY 1

Genera of Phytopathogenic Fungi (GOPHY) is introduced as a new series of publications in order to provide a stable platform for the taxonomy of phytopathogenic fungi. This first paper focuses on 21 genera of phytopathogenic fungi: Bipolaris, Boeremia, Calonectria, Ceratocystis, Cladosporium, Colletotrichum, Coniella, Curvularia, Monilinia, Neofabraea, Neofusicoccum, Pilidium, Pleiochaeta, Plenodomus, Protostegia, Pseudopyricularia, Puccinia, Saccharata, Thyrostroma, Venturia and Wilsonomyces. For each genus, a morphological description and information about its pathology, distribution, hosts and disease symptoms are provided. In addition, this information is linked to primary and secondary DNA barcodes of the presently accepted species, and relevant literature. Moreover, several novelties are introduced, i.e. new genera, species and combinations, and neo-, lecto- and epitypes designated to provide a stable taxonomy. This first paper includes one new genus, 26 new species, nine new combinations, and four typifications of older names

Congenital leptin deficiency and leptin gene missense mutation found in two colombian sisters with severe obesity

Background: Congenital leptin deficiency is a recessive genetic disorder associated with severe early-onset obesity. It is caused by mutations in the leptin (LEP) gene, which encodes the protein product leptin. These mutations may cause nonsense-mediated mRNA decay, defective secretion or the phenomenon of biologically inactive leptin, but typically lead to an absence of circulating leptin, resulting in a rare type of monogenic extreme obesity with intense hyperphagia, and serious metabolic abnormalities. Methods: We present two severely obese sisters from Colombia, members of the same lineal consanguinity. Their serum leptin was measured by MicroELISA. DNA sequencing was performed on MiSeq equipment (Illumina) of a next-generation sequencing (NGS) panel involving genes related to severe obesity, including LEP. Results: Direct sequencing of the coding region of LEP gene in the sisters revealed a novel homozygous missense mutation in exon 3 [NM_002303.3], C350G>T [p.C117F]. Detailed information and clinical measurements of these sisters were also collected. Their serum leptin levels were undetectable despite their markedly elevated fat mass. Conclusions: The mutation of LEP, absence of detectable leptin, and the severe obesity found in these sisters provide the first evidence of monogenic leptin deficiency reported in the continents of North and South America. © 2019 by the authors. Licensee MDPI, Basel, Switzerland

The genera of fungi-fixing the application of the type species of generic names-G 2: Allantophomopsis, Latorua, Macrodiplodiopsis, Macrohilum, Milospium, Protostegia, Pyricularia, Robillarda, Rotula, Septoriella, Torula, and Wojnowicia

The present paper represents the second contribution in the Genera of Fungi series, linking type species of fungal genera to their morphology and DNA sequence data, and where possible, ecology. This paper focuses on 12 genera of microfungi, 11 of which the type species are neo- or epitypified here: Allantophomopsis (A. cytisporea, Phacidiaceae, Phacidiales, Leotiomycetes), Latorua gen. nov. (Latorua caligans, Latoruaceae, Pleosporales, Dothideomycetes), Macrodiplodiopsis (M. desmazieri, Macrodiplodiopsidaceae, Pleosporales, Dothideomycetes), Macrohilum (M. eucalypti, Macrohilaceae, Diaporthales, Sordariomycetes), Milospium (M. graphideorum, incertae sedis, Pezizomycotina), Protostegia (P. eucleae, Mycosphaerellaceae, Capnodiales, Dothideomycetes), Pyricularia (P. grisea, Pyriculariaceae, Magnaporthales, Sordariomycetes), Robillarda (R. sessilis, Robillardaceae, Xylariales, Sordariomycetes), Rutola (R. graminis, incertae sedis, Pleosporales, Dothideomycetes), Septoriella (S. phragmitis, Phaeosphaeriaceae, Pleosporales, Dothideomycetes), Torula (T. herbarum, Torulaceae, Pleosporales, Dothideomycetes) and Wojnowicia (syn. of Septoriella, S. hirta, Phaeosphaeriaceae, Pleosporales, Dothideomycetes). Novel species include Latorua grootfonteinensis, Robillarda africana, R. roystoneae, R. terrae, Torula ficus, T. hollandica, and T. masonii spp. nov., and three new families: Macrodiplodiopsisceae, Macrohilaceae, and Robillardaceae. Authors interested in contributing accounts of individual genera to larger multi-authored papers to be published in IMA Fungus, should contact the associate editors listed for the major groups of fungi on the List of Protected Generic Names for FungiThe Austrian Science Fund (FWF; project P25870-B16)http://www.generaoffungi.orgam201

Antimicrobial resistance among migrants in Europe: a systematic review and meta-analysis

BACKGROUND: Rates of antimicrobial resistance (AMR) are rising globally and there is concern that increased migration is contributing to the burden of antibiotic resistance in Europe. However, the effect of migration on the burden of AMR in Europe has not yet been comprehensively examined. Therefore, we did a systematic review and meta-analysis to identify and synthesise data for AMR carriage or infection in migrants to Europe to examine differences in patterns of AMR across migrant groups and in different settings. METHODS: For this systematic review and meta-analysis, we searched MEDLINE, Embase, PubMed, and Scopus with no language restrictions from Jan 1, 2000, to Jan 18, 2017, for primary data from observational studies reporting antibacterial resistance in common bacterial pathogens among migrants to 21 European Union-15 and European Economic Area countries. To be eligible for inclusion, studies had to report data on carriage or infection with laboratory-confirmed antibiotic-resistant organisms in migrant populations. We extracted data from eligible studies and assessed quality using piloted, standardised forms. We did not examine drug resistance in tuberculosis and excluded articles solely reporting on this parameter. We also excluded articles in which migrant status was determined by ethnicity, country of birth of participants' parents, or was not defined, and articles in which data were not disaggregated by migrant status. Outcomes were carriage of or infection with antibiotic-resistant organisms. We used random-effects models to calculate the pooled prevalence of each outcome. The study protocol is registered with PROSPERO, number CRD42016043681. FINDINGS: We identified 2274 articles, of which 23 observational studies reporting on antibiotic resistance in 2319 migrants were included. The pooled prevalence of any AMR carriage or AMR infection in migrants was 25·4% (95% CI 19·1-31·8; I2 =98%), including meticillin-resistant Staphylococcus aureus (7·8%, 4·8-10·7; I2 =92%) and antibiotic-resistant Gram-negative bacteria (27·2%, 17·6-36·8; I2 =94%). The pooled prevalence of any AMR carriage or infection was higher in refugees and asylum seekers (33·0%, 18·3-47·6; I2 =98%) than in other migrant groups (6·6%, 1·8-11·3; I2 =92%). The pooled prevalence of antibiotic-resistant organisms was slightly higher in high-migrant community settings (33·1%, 11·1-55·1; I2 =96%) than in migrants in hospitals (24·3%, 16·1-32·6; I2 =98%). We did not find evidence of high rates of transmission of AMR from migrant to host populations. INTERPRETATION: Migrants are exposed to conditions favouring the emergence of drug resistance during transit and in host countries in Europe. Increased antibiotic resistance among refugees and asylum seekers and in high-migrant community settings (such as refugee camps and detention facilities) highlights the need for improved living conditions, access to health care, and initiatives to facilitate detection of and appropriate high-quality treatment for antibiotic-resistant infections during transit and in host countries. Protocols for the prevention and control of infection and for antibiotic surveillance need to be integrated in all aspects of health care, which should be accessible for all migrant groups, and should target determinants of AMR before, during, and after migration. FUNDING: UK National Institute for Health Research Imperial Biomedical Research Centre, Imperial College Healthcare Charity, the Wellcome Trust, and UK National Institute for Health Research Health Protection Research Unit in Healthcare-associated Infections and Antimictobial Resistance at Imperial College London

Fungal Planet description sheets: 785– 867

Novel species of fungi described in this study include those from various countries as follows: Angola, Gnomoniopsis angolensis and Pseudopithomyces angolensis on unknown host plants. Australia, Dothiora corymbiae on Corymbia citriodora, Neoeucasphaeria eucalypti (incl. Neoeucasphaeria gen. nov.)on Eucalyptus sp., Fumagopsis stellae on Eucalyptus sp., Fusculina eucalyptorum (incl. Fusculinaceae fam. nov.) on Eucalyptus socialis, Harknessia corymbiicola on Corymbia maculata, Neocelosporium eucalypti (incl. Neocelosporium gen. nov., Neocelosporiaceae fam. nov. and Neocelosporiales ord. nov.) on Eucalyptus cyanophylla, Neophaeomoniella corymbiae on Corymbia citriodora, Neophaeomoniella eucalyptigena on Eucalyptus pilularis, Pseudoplagiostoma corymbiicola on Corymbia citriodora, Teratosphaeria gracilis on Eucalyptus gracilis, Zasmidium corymbiae on Corymbia citriodora. Brazil, Calonectria hemileiae on pustules of Hemileia vastatrix formed on leaves of Coffea arabica, Calvatia caatinguensis on soil, Cercospora solani-betacei on Solanum betaceum, Clathrus natalensis on soil, Diaporthe poincianellae on Poincianella pyramidalis, Geastrum piquiriunense on soil, Geosmithia carolliae on wing of Carollia perspicillata, Henningsia resupinata on wood, Penicillium guaibinense from soil, Periconia caespitosa from leaf litter, Pseudocercospora styracina on Styrax sp., Simplicillium filiforme as endophyte from Citrullus lanatus, Thozetella pindobacuensis on leaf litter, Xenosonderhenia coussapoae on Coussapoa floccosa. Canary Islands (Spain), Orbilia amarilla on Euphorbia canariensis. Cape Verde Islands, Xylodon jacobaeus on Eucalyptus camaldulensis. Chile, Colletotrichum arboricola on Fuchsia magellanica. Costa Rica, Lasiosphaeria miniovina ontreebranch. Ecuador, Ganoderma chocoense ontreetrunk. France, Neofitzroyomyces nerii (incl. Neofitzroyomyces gen. nov.) on Nerium oleander. Ghana, Castanediella tereticornis on Eucalyptus tereticornis, Falcocladium africanum on Eucalyptus brassiana, Rachicladosporium corymbiae on Corymbia citriodora. Hungary, Entoloma silvae-frondosae in Carpinus betulus-Pinus sylvestris mixedforest. Iran, Pseudopyricularia persiana on Cyperus sp. Italy, Inocybe roseascens onsoilinmixedforest. Laos, Ophiocordyceps houaynhangensis on Coleoptera larva. Malaysia, Monilochaetes melastomae on Melastoma sp. Mexico, Absidia terrestris fromsoil. Netherlands, Acaulium pannemaniae, Conioscypha boutwelliae, Fusicolla septimanifiniscientiae, Gibellulopsis simonii, Lasionectria hilhorstii, Lectera nordwiniana, Leptodiscella rintelii, Parasarocladium debruynii and Sarocladium dejongiae (incl. Sarocladiaceae fam. nov.) fromsoil. New Zealand, Gnomoniopsis rosae on Rosa sp. and Neodevriesia metrosideri on Metrosideros sp. Puerto Rico, Neodevriesia coccolobae on Coccoloba uvifera, Neodevriesia tabebuiae and Alfaria tabebuiae on Tabebuia chrysantha . Russia, Amanita paludosa on bogged soil in mixed deciduous forest, Entoloma tiliae in forest of Tilia × europaea, Kwoniella endophytica on Pyrus communis. South Africa, Coniella diospyri on Diospyros mespiliformis, Neomelanconiella combreti (incl. Neomelanconiellaceae fam. nov. and Neomelanconiella gen. nov.)on Combretum sp., Polyphialoseptoria natalensis on unidentified plant host, Pseudorobillarda bolusanthi on Bolusanthus speciosus, Thelonectria pelargonii on Pelargonium sp. Spain, Vermiculariopsiella lauracearum and Anungitopsis lauri on Laurus novocanariensis, Geosmithia xerotolerans from a darkened wall of a house, Pseudopenidiella gallaica on leaf litter. Thailand, Corynespora thailandica on wood, Lareunionomyces loeiensis on leaf litter, Neocochlearomyces chromolaenae (incl. Neocochlearomyces gen. nov.) on Chromolaena odorata, Neomyrmecridium septatum (incl. Neomyrmecridium gen. nov .), Pararamichloridium caricicola on Carex sp., Xenodactylaria thailandica (incl. Xenodactylariaceae fam. nov. and Xenodactylaria gen. nov.), Neomyrmecridium asiaticum and Cymostachys thailandica fromunidentifiedvine. USA, Carolinigaster bonitoi (incl. Carolinigaster gen. nov.)fromsoil, Penicillium fortuitum from house dust, Phaeotheca shathenatiana (incl. Phaeothecaceae fam. nov.) from twig and cone litter, Pythium wohlseniorum from stream water, Superstratomyces tardicrescens from human eye, Talaromyces iowaense from officeair. Vietnam, Fistulinella olivaceoalba onsoil. Morphological and culture characteristics along with DNA barcodes are provided Novel species of fungi described in this study include those from various countries as follows: Angola, Gnomoniopsis angolensis and Pseudopithomyces angolensis on unknown host plants. Australia, Dothiora corymbiae on Corymbia citriodora, Neoeucasphaeria eucalypti (incl. Neoeucasphaeria gen. nov.)on Eucalyptus sp., Fumagopsis stellae on Eucalyptus sp., Fusculina eucalyptorum (incl. Fusculinaceae fam. nov.) on Eucalyptus socialis, Harknessia corymbiicola on Corymbia maculata, Neocelosporium eucalypti (incl. Neocelosporium gen. nov., Neocelosporiaceae fam. nov. and Neocelosporiales ord. nov.) on Eucalyptus cyanophylla, Neophaeomoniella corymbiae on Corymbia citriodora, Neophaeomoniella eucalyptigena on Eucalyptus pilularis, Pseudoplagiostoma corymbiicola on Corymbia citriodora, Teratosphaeria gracilis on Eucalyptus gracilis, Zasmidium corymbiae on Corymbia citriodora. Brazil, Calonectria hemileiae on pustules of Hemileia vastatrix formed on leaves of Coffea arabica, Calvatia caatinguensis on soil, Cercospora solani-betacei on Solanum betaceum, Clathrus natalensis on soil, Diaporthe poincianellae on Poincianella pyramidalis, Geastrum piquiriunense on soil, Geosmithia carolliae on wing of Carollia perspicillata, Henningsia resupinata on wood, Penicillium guaibinense from soil, Periconia caespitosa from leaf litter, Pseudocercospora styracina on Styrax sp., Simplicillium filiforme as endophyte from Citrullus lanatus, Thozetella pindobacuensis on leaf litter, Xenosonderhenia coussapoae on Coussapoa floccosa. Canary Islands (Spain), Orbilia amarilla on Euphorbia canariensis. Cape Verde Islands, Xylodon jacobaeus on Eucalyptus camaldulensis. Chile, Colletotrichum arboricola on Fuchsia magellanica. Costa Rica, Lasiosphaeria miniovina ontreebranch. Ecuador, Ganoderma chocoense ontreetrunk. France, Neofitzroyomyces nerii (incl. Neofitzroyomyces gen. nov.) on Nerium oleander. Ghana, Castanediella tereticornis on Eucalyptus tereticornis, Falcocladium africanum on Eucalyptus brassiana, Rachicladosporium corymbiae on Corymbia citriodora. Hungary, Entoloma silvae-frondosae in Carpinus betulus-Pinus sylvestris mixedforest. Iran, Pseudopyricularia persiana on Cyperus sp. Italy, Inocybe roseascens onsoilinmixedforest. Laos, Ophiocordyceps houaynhangensis on Coleoptera larva. Malaysia, Monilochaetes melastomae on Melastoma sp. Mexico, Absidia terrestris fromsoil. Netherlands, Acaulium pannemaniae, Conioscypha boutwelliae, Fusicolla septimanifiniscientiae, Gibellulopsis simonii, Lasionectria hilhorstii, Lectera nordwiniana, Leptodiscella rintelii, Parasarocladium debruynii and Sarocladium dejongiae (incl. Sarocladiaceae fam. nov.) fromsoil. New Zealand, Gnomoniopsis rosae on Rosa sp. and Neodevriesia metrosideri on Metrosideros sp. Puerto Rico, Neodevriesia coccolobae on Coccoloba uvifera, Neodevriesia tabebuiae and Alfaria tabebuiae on Tabebuia chrysantha. Russia, Amanita paludosa on bogged soil in mixed deciduous forest, Entoloma tiliae in forest of Tilia × europaea, Kwoniella endophytica on Pyrus communis. South Africa, Coniella diospyri on Diospyros mespiliformis, Neomelanconiella combreti (incl. Neomelanconiellaceae fam. nov. and Neomelanconiella gen. nov.)on Combretum sp., Polyphialoseptoria natalensis on unidentified plant host, Pseudorobillarda bolusanthi on Bolusanthus speciosus, Thelonectria pelargonii on Pelargonium sp. Spain, Vermiculariopsiella lauracearum and Anungitopsis lauri on Laurus novocanariensis, Geosmithia xerotolerans from a darkened wall of a house, Pseudopenidiella gallaica on leaf litter. Thailand, Corynespora thailandica on wood, Lareunionomyces loeiensis on leaf litter, Neocochlearomyces chromolaenae (incl. Neocochlearomyces gen. nov.) on Chromolaena odorata, Neomyrmecridium septatum (incl. Neomyrmecridium gen. nov .), Pararamichloridium caricicola on Carex sp., Xenodactylaria thailandica (incl. Xenodactylariaceae fam. nov. and Xenodactylaria gen. nov.), Neomyrmecridium asiaticum and Cymostachys thailandica fromunidentifiedvine. USA, Carolinigaster bonitoi (incl. Carolinigaster gen. nov.)fromsoil, Penicillium fortuitum from house dust, Phaeotheca shathenatiana (incl. Phaeothecaceae fam. nov.) from twig and cone litter, Pythium wohlseniorum from stream water, Superstratomyces tardicrescens from human eye, Talaromyces iowaense from officeair. Vietnam, Fistulinella olivaceoalba onsoil. Morphological and culture characteristics along with DNA barcodes are provided