2021 Taxonomic update of phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales.

Correction to: 2021 Taxonomic update of phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales. Archives of Virology (2021) 166:3567–3579. https://doi.org/10.1007/s00705-021-05266-wIn March 2021, following the annual International Committee on Taxonomy of Viruses (ICTV) ratification vote on newly proposed taxa, the phylum Negarnaviricota was amended and emended. The phylum was expanded by four families (Aliusviridae, Crepuscuviridae, Myriaviridae, and Natareviridae), three subfamilies (Alpharhabdovirinae, Betarhabdovirinae, and Gammarhabdovirinae), 42 genera, and 200 species. Thirty-nine species were renamed and/or moved and seven species were abolished. This article presents the updated taxonomy of Negarnaviricota as now accepted by the ICTV.This work was supported in part through Laulima Government Solutions, LLC prime contract with the US National Institute of Allergy and Infectious Diseases (NIAID) under Contract No. HHSN272201800013C. J.H.K. performed this work as an employee of Tunnell Government Services (TGS), a subcontractor of Laulima Government Solutions, LLC under Contract No. HHSN272201800013C. This work was also supported in part with federal funds from the National Cancer Institute (NCI), National Institutes of Health (NIH), under Contract No. 75N91019D00024, Task Order No. 75N91019F00130 to I.C., who was supported by the Clinical Monitoring Research Program Directorate, Frederick National Lab for Cancer Research. This work was also funded in part by Contract No. HSHQDC-15-C-00064 awarded by DHS S&T for the management and operation of The National Biodefense Analysis and Countermeasures Center, a federally funded research and development center operated by the Battelle National Biodefense Institute (V.W.); and NIH contract HHSN272201000040I/HHSN27200004/D04 and grant R24AI120942 (N.V., R.B.T.). S.S. acknowledges partial support from the Special Research Initiative of Mississippi Agricultural and Forestry Experiment Station (MAFES), Mississippi State University, and the National Institute of Food and Agriculture, US Department of Agriculture, Hatch Project 1021494. Part of this work was supported by the Francis Crick Institute which receives its core funding from Cancer Research UK (FC001030), the UK Medical Research Council (FC001030), and the Wellcome Trust (FC001030).S

2021 Taxonomic update of phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales.

In March 2021, following the annual International Committee on Taxonomy of Viruses (ICTV) ratification vote on newly proposed taxa, the phylum Negarnaviricota was amended and emended. The phylum was expanded by four families (Aliusviridae, Crepuscuviridae, Myriaviridae, and Natareviridae), three subfamilies (Alpharhabdovirinae, Betarhabdovirinae, and Gammarhabdovirinae), 42 genera, and 200 species. Thirty-nine species were renamed and/or moved and seven species were abolished. This article presents the updated taxonomy of Negarnaviricota as now accepted by the ICTV

Daily intake of a bean-fiber fortified bar reduces oxidative stress

It has been proposed that the consumption of common beans (Phaseolus vulgaris L.) reduces cardiovascular risk, and prevents and controls both chronic and degenerative diseases. The aim of this study was to compare the antioxidant capacity of a bean-fiber fortified bar (BFB) versus a commercial bar (CB) in 60 Mexican men and women (18-65 years old), who were randomly distributed in two groups: BFB or CB; individuals consumed a bar a day for one month. Anthropometric data, food intake and blood samples were collected. Glucose tolerance (GTT), lipid profile (PL), and lipid peroxidation (TBARS) tests were performed; carbonyls groups in serum oxidized proteins were also measured. GTT and PL were not different between both groups in either the 15 or 30-day follow-up of bar consumption assessments. There were no significant differences in either TBARS or carbonyl concentration between groups; BFB group showed higher levels of serum lipid peroxidation in basal and fifteen days measurements; these levels decreased at the final evaluation: No differences were detected on carbonyl levels between groups. In conclusion, 30 days of fiber bean bar consumption did not alter glucose or PL levels, while, in the BFF group, oxidative stress decreased within 30 days of the consumption of the fortified bar.Se ha propuesto que el consumo de frijol común (Phaseolus vulgaris L.) reduce el riesgo cardiovascular, y previene y controla las enfermedades crónicas y degenerativas. El objetivo del presente estudio fue comparar la capacidad antioxidante de una barra fortificada con fibra de frijol (BFB) versus una barra comercial (CB) en 60 hombres y mujeres mexicanos (18-65 años de edad), quienes aleatoriamente fueron distribuidos en dos grupos: El grupo BFB y el CB que consumieron la barras fortificada con frijol y la barra comercial, respectivamente, durante un mes. Se recopilaron datos antropométricos, ingesta de alimentos y muestras de sangre. Se realizó prueba de tolerancia a la glucosa (GTT), el perfil de lípidos (PL), la peroxidación de lípidos (TBARS) y la cuantificación de carbonilos en proteínas oxidadas como pruebas de bioquímica sanguínea. GTT y PL no fueron diferentes entre ambos grupos en la evaluación de seguimiento de 15 y 30 días del consumo de la barra. No hubo diferencias significativas en los TBARS o la concentración de carbonilo entre los grupos, el grupo BFB mostró niveles más altos de peroxidación de lípidos en suero en la fase basal y a los quince días del consumo de la barra; curiosamente, estos niveles disminuyeron en la evaluación final. No se detectaron diferencias en los niveles de carbonilo entre los grupos. En conclusión, 30 días de consumo de barras de fibra de frijol no alteraron los niveles de glucosa o PL; mientras que, en el grupo BFB, el estrés oxidativo disminuyó a los 30 días del consumo de la barra fortificada

Embryonic and larval development of Eugerres mexicanus (Perciformes: Gerreidae) in Tenosique: Tabasco, Mexico

Most studies on Eugerres mexicanus mainly consider biogeographic and systematic aspects and rarely address reproductive characteristics, which are useful for fishery population management plans. This study aimed at evaluating the ontogeny of E. mexicanus, based on 30 embryos and 30 larvae sampled by induced spawning of breeders, taken in February 2009 from the Usumacinta River in Tenosique, Tabasco, Mexico. All descriptions of the embryonic development were based on morphometric and meristic data and followed standard methods. Eggs, recovered at the gastrula stage, had an average diameter of 1.17mm (SD=0.08). The bud stage appeared during the first three hours of development, in which the posterior side was adhered to the vitellus; Kupffer´s vesicle was visible. Yolk-sac larvae hatched 18 hours after fertilization, exhibiting a light brown color and an average total length of 2.94mm (SD=0.70); the preflexion stage was reached eight days after hatching, with a total average length of 4.67mm (SD=0.50) and a total notochord length of 4.45mm (SD=0.50). The flexion stage was reached on the 16th day, with an average total length of 6.66mm (SD=1.53), while postflexion was reached on the 24th day, with 10.33mm (SD=1.45). The pre-juvenile stage was reached on the 33rd day, with a total length of 14.30mm (SD=0.93), showing IX spines and 10 rays and III spines and eight rays in the dorsal and anal fins, respectively. The juvenile stage was reached by the 45th day, with an average length of 28.16mm (SD=1.93) and average weight of 4.75g (SD=1.49). Prejuveniles showed an initial pigmentation with dark colored dots in the superior and inferior jaw and dispersed on the head, while juveniles presented the same pigmentation pattern, decreasing towards the margin of the caudal peduncle. In conclusion, the embryonic developmental stages of E. mexicanus were typical for the Gerreidae group. However, their morphometric characters were slightly different since the diameter and size of the drop of oil were bigger than those reported for marine species. In addition, regarding pigmentation, the yolk-sac larvae of E. mexicanus were olive and yellow on the margin of the notochord, which differs from those reported for other species. This is the first recorded report on the reproductive biology and early life development of this species.<br>La ontogenia se basó en 30 embriones y 30 larvas, obtenidos mediante la inducción del desove de reproductores provenientes de la ribera del río Usumacinta en Tenosique, Tabasco, México, recolectados en febrero de 2009. La descripción se fundamentó en el registro morfométrico y merístico. Los huevos fueron recuperados en estado de gástrula y presentaron un diámetro de promedio de 1.17mm (SD=0.08). Durante las primeras tres horas de desarrollo embrionario, se presentó la etapa de capullo, en la que se observó la región caudal adherida al vitelo, apreciándose la vesícula de Kupffer. Las larvas con saco eclosionaron a las 18 horas pos-fertilización, fueron de color marrón claro con un promedio de 2.94mm; (SD=0.70) de longitud total y alcanzaron la preflexión a los ocho días post-eclosión con una longitud total promedio de 4.67mm; (SD=0.50) y una longitud total del notocordio de 4.45; (SD=0.50). A los 16 días de la eclosión alcanzaron la flexión, con un promedio de 6.66mm; (SD=1.53) de longitud total. La postflexión se presentó a los 24 días con 10.33mm; (SD=1.45). Al llegar a los 33 días, se presentó la fase prejuvenil y llegaron a medir 14.30; (SD=0.93) de longitud total, presentando IX espinas y 10 radios en la aleta dorsal y III y ocho en la aleta anal. Los juveniles midieron 28.16; (SD=1.93) de longitud a los 45 días, con un peso promedio de 4.75g; (SD=1.49). Los prejuveniles presentaron una pigmentación inicial en la mandíbula superior e inferior con tintes oscuros en forma de puntos y de manera dispersa sobre la cabeza. En los juveniles se observó el mismo patrón de pigmentación, disminuyendo hacia el margen del pedúnculo caudal. Las características descriptivas de la etapa de desarrollo embrionario de E. mexicanus son típicas del período de desarrollo de los peces de la familia Gerreidae, en particular en el caso de las especies E. brasilianus y E. lineatus que habitan en ambientes marinos. Sin embargo, sus caracteres morfométricos son diferentes con respecto al diámetro y el tamaño de los huevos y de la gota de aceite, ya que en E. mexicanus son más grandes que los de las especies marinas y son similares a los de los peces de agua dulce. Con respecto a la pigmentación, la larva con saco de E. mexicanus presenta un olor olivo y amarillo sobre el margen del notocordio, lo cual difiere a lo reportado para E. lineatus,ya que en esta muestra un grupo de melanóforos entre los miomeros nueve al 13 como principal característica, y para Diapturus peruvianus por presentar tres manchas en el margen dorsal de los intestinos desde la inserción de la aleta pectoral hasta el ano. Los resultados de este estudio son los primeros registrados para esta especie y han generado información sobre aspectos de su biología reproductiva y el desarrollo de la vida temprana

Embryonic and larval development of Eugerres mexicanus (Perciformes: Gerreidae) in Tenosique, Tabasco, Mexico.

Most studies on Eugerres mexicanus mainly consider biogeographic and systematic aspects and rarely address reproductive characteristics, which are useful for fishery population management plans. This study aimed at evaluating the ontogeny of E. mexicanus, based on 30 embryos and 30 larvae sampled by induced spawning of breeders, taken in February 2009 from the Usumacinta River in Tenosique, Tabasco, Mexico. All descriptions of the embryonic development were based on morphometric and meristic data and followed standard methods. Eggs, recovered at the gastrula stage, had an average diameter of 1.17mm (SD=0.08). The bud stage appeared during the first three hours of development, in which the posterior side was adhered to the vitellus; Kupffer's vesicle was visible. Yolk-sac larvae hatched 18 hours after fertilization, exhibiting a light brown color and an average total length of 2.94mm (SD=0.70); the preflexion stage was reached eight days after hatching, with a total average length of 4.67mm (SD=0.50) and a total notochord length of 4.45mm (SD=0.50). The flexion stage was reached on the 16th day, with an average total length of 6.66mm (SD=1.53), while postflexion was reached on the 24th day, with 10.33mm (SD=1.45). The pre-juvenile stage was reached on the 33rd day, with a total length of 14.30mm (SD=0.93), showing IX spines and 10 rays and III spines and eight rays in the dorsal and anal fins, respectively. The juvenile stage was reached by the 45th day, with an average length of 28.16mm (SD=1.93) and average weight of 4.75g (SD=1.49). Prejuveniles showed an initial pigmentation with dark colored dots in the superior and inferior jaw and dispersed on the head, while juveniles presented the same pigmentation pattern, decreasing towards the margin of the caudal peduncle. In conclusion, the embryonic developmental stages of E. mexicanus were typical for the Gerreidae group. However, their morphometric characters were slightly different since the diameter and size of the drop of oil were bigger than those reported for marine species. In addition, regarding pigmentation, the yolk-sac larvae of E. mexicanus were olive and yellow on the margin of the notochord, which differs from those reported for other species. This is the first recorded report on the reproductive biology and early life development of this species.La ontogenia se basó en 30 embriones y 30 larvas, obtenidos mediante la inducción del desove de reproductores provenientes de la ribera del río Usumacinta en Tenosique, Tabasco, México, recolectados en febrero de 2009. La descripción se fundamentó en el registro morfométrico y merístico. Los huevos fueron recuperados en estado de gástrula y presentaron un diámetro de promedio de 1.17mm (SD=0.08). Durante las primeras tres horas de desarrollo embrionario, se presentó la etapa de capullo, en la que se observó la región caudal adherida al vitelo, apreciándose la vesícula de Kupffer. Las larvas con saco eclosionaron a las 18 horas pos-fertilización, fueron de color marrón claro con un promedio de 2.94mm; (SD=0.70) de longitud total y alcanzaron la preflexión a los ocho días post-eclosión con una longitud total promedio de 4.67mm; (SD=0.50) y una longitud total del notocordio de 4.45; (SD=0.50). A los 16 días de la eclosión alcanzaron la flexión, con un promedio de 6.66mm; (SD=1.53) de longitud total. La postflexión se presentó a los 24 días con 10.33mm; (SD=1.45). Al llegar a los 33 días, se presentó la fase prejuvenil y llegaron a medir 14.30; (SD=0.93) de longitud total, presentando IX espinas y 10 radios en la aleta dorsal y III y ocho en la aleta anal. Los juveniles midieron 28.16; (SD=1.93) de longitud a los 45 días, con un peso promedio de 4.75g; (SD=1.49). Los prejuveniles presentaron una pigmentación inicial en la mandíbula superior e inferior con tintes oscuros en forma de puntos y de manera dispersa sobre la cabeza. En los juveniles se observó el mismo patrón de pigmentación, disminuyendo hacia el margen del pedúnculo caudal. Las características descriptivas de la etapa de desarrollo embrionario de E. mexicanus son típicas del período de desarrollo de los peces de la familia Gerreidae, en particular en el caso de las especies E. brasilianus y E. lineatus que habitan en ambientes marinos. Sin embargo, sus caracteres morfométricos son diferentes con respecto al diámetro y el tamaño de los huevos y de la gota de aceite, ya que en E. mexicanus son más grandes que los de las especies marinas y son similares a los de los peces de agua dulce. Con respecto a la pigmentación, la larva con saco de E. mexicanus presenta un olor olivo y amarillo sobre el margen del notocordio, lo cual difiere a lo reportado para E. lineatus, ya que en esta muestra un grupo de melanóforos entre los miomeros nueve al 13 como principal característica, y para Diapturus peruvianus por presentar tres manchas en el margen dorsal de los intestinos desde la inserción de la aleta pectoral hasta el ano. Los resultados de este estudio son los primeros registrados para esta especie y han generado información sobre aspectos de su biología reproductiva y el desarrollo de la vida temprana

The role of monk parakeets as nest-site facilitators in their native and invaded areas

While most of the knowledge on invasive species focuses on their impacts, little is known about their potential positive effects on other species. Invasive ecosystem engineers can disrupt recipient environments; however, they may also facilitate access to novel resources for native species. The monk parakeet (Myiopsitta monachus) is a worldwide invader and the only parrot that builds its own communal nests, which can be used by other species. However, the ecological effects of these interspecific interactions are barely known. We compared the role of the monk parakeet as a nest-site facilitator in different rural and urban areas, both invaded and native, across three continents and eight breeding seasons. A total of 2690 nests from 42 tenant species, mostly cavity-nesting birds, were recorded in 26% of 2595 monk parakeet nests. Rural and invaded areas showed the highest abundance and richness of tenant species. Multispecies communal nests triggered interspecific aggression between the monk parakeet host and its tenants, but also a cooperative defense against predators. Despite the positive effects for native species, monk parakeets also facilitate nesting opportunities to other non-native species and may also transmit diseases to tenants, highlighting the complexity of biotic interactions in biological invasions

The Role of Monk Parakeets as Nest-Site Facilitators in Their Native and Invaded Areas

While most of the knowledge on invasive species focuses on their impacts, little is known about their potential positive effects on other species. Invasive ecosystem engineers can disrupt recipient environments; however, they may also facilitate access to novel resources for native species. The monk parakeet (Myiopsitta monachus) is a worldwide invader and the only parrot that builds its own communal nests, which can be used by other species. However, the ecological effects of these interspecific interactions are barely known. We compared the role of the monk parakeet as a nest-site facilitator in different rural and urban areas, both invaded and native, across three continents and eight breeding seasons. A total of 2690 nests from 42 tenant species, mostly cavity-nesting birds, were recorded in 26% of 2595 monk parakeet nests. Rural and invaded areas showed the highest abundance and richness of tenant species. Multispecies communal nests triggered interspecific aggression between the monk parakeet host and its tenants, but also a cooperative defense against predators. Despite the positive effects for native species, monk parakeets also facilitate nesting opportunities to other non-native species and may also transmit diseases to tenants, highlighting the complexity of biotic interactions in biological invasions.This research was funded by Severo Ochoa Program (SVP-2014-068732), Action COST “ParrotNet” (ES1304), Loro Parque Fundación (PP-146-2018-1), and Ministry of Economy and Competitiveness, Spanish Research Council (CGL-2016-79568-C3-3-P).Peer reviewe

Integrating climate adaptation and transboundary management:Guidelines for designing climate-smart marine protected areas

Climate change poses an urgent threat to biodiversity that demands societal responses. The magnitude of this challenge is reflected in recent international commitments to protect 30% of the planet by 2030 while adapting to climate change. However, because climate change is global, interventions must transcend political boundaries. Here, using the California Bight as a case study, we provide 21 biophysical guidelines for designing climate-smart transboundary marine protected area (MPA) networks and conduct analyses to inform their application. We found that future climates and marine heatwaves could decrease ecological connectivity by 50% and hinder the recovery of vulnerable species in MPAs. To buffer the impacts of climate change, MPA coverage should be expanded, focusing on protecting critical nodes for the network and climate refugia, where impacts might be less severe. For shared ecoregions, these actions require international coordination. Our work provides the first comprehensive framework for integrating climate resilience for MPAs in transboundary ecoregions, which will support other nations’ aspirations.</p