COLECTAPP: Herramienta Aplicada al Área de la Biología

COLECTAPP fue desarrollada para facilitar y optimizar la tarea de colecta de datos a través del uso de dispositivos como Smartphone y tabletas utilizando los sensores y cámaras que vienen incluidos en estos, por medio de los servicios de ubicación basados en internet y dispositivos GPS se puede obtener la ubicación en tiempo real, la captura de información es a través de interfaces y el uso de los manejadores de bases de datos embebidos; es una aplicación creada para la plataforma de dispositivos móviles Android, bajo el lenguaje de programación java, utilizando los más recientes entornos de desarrollo para dicha plataforma, ésta incorpora el uso de las bases de datos para el almacenamiento de la información como es Sqlite, por su naturaleza se puede utilizar los servicios de ubicación basados en internet y sin ellos, gracias al diseño de su interfaz permite al usuario la captura de información, fotografías, generación de mapas, consulta de información y fotografías referentes a la colecta ya registrada, eliminar o enviar la información a un servidor web a través de un web service haciendo uso de la arquitectura cliente servidor aprovechando las características del formato JSON y las conexiones a internet

Urinary Excretion of Mimosine Derivatives by Cows with and without Experience in Consumption of \u3cem\u3eLeucaena leucocephala\u3c/em\u3e

Leucaena leucocephala is a leguminous tree widely distributed in the tropical regions of the world. In Mexico, it has been incorporated into silvopastoral systems and is highly regarded, owing to its high content of crude protein. Nonetheless, L. leucocephala contains secondary metab-olites, such as mimosine, a non-protein free amino acid, which may induce toxic effects in unadapted ruminants that consume the forage (Hammond 1995). Although Synergistes jonesii, an anaerobic bacterium, has the ability to degrade 3,4-DHP and 2,3-DHP to non-toxic compounds (Allison et al. 1992), in Mexico its presence has not yet been confirmed. Recent work has suggested the occurrence of sub-clinical toxicity to 3,4-DHP and 2,3-DHP in cattle grazing L. leucocephala in Australia and Thailand (Graham 2007; Dalzell et al. 2012; Phaikaew et al. 2012). Several options such as the transfer of rumen liquor and the adaptation of ruminants to the intake of L. leucocephala have been studied in an attempt to reduce the excretion of mimosine and its metabolites (Palmer et al. 2010). The aim of the present work was to evaluate the effect of the experience of consumption of L. leucocephala on excretion of mimosine derivatives (3,4-DHP and 2,3-DHP) in the urine of cattle

Productive Performance of Growing Cattle Grazing a Silvopastoral System with \u3cem\u3eLeucaena leucocephala\u3c/em\u3e

In tropical regions, the feeding of cattle is usually based on the grazing of medium to low quality grasses. Low fertility of soils, changing climatic conditions and the poor management of pastures, have further reduced the quality and forage yield of pastures. The low availability and quality of grasses gives modest weight gains for grazing cattle and this in-turn causes low economical efficiency of cattle production systems (Campos et al. 2011). Silvopastoral systems represent a sustainable option for meat and milk production in the tropics. The association of grasses with legumes such as Leucaena leucocephala (leucaena) supply forage with high concentration of crude protein (Barros et al. 2012). There are reports in the scientific literature which show that intake of leucaena can result in good rates of growth in cattle (e.g. Shelton and Dalzell 2007); however the presence of the free amino acid mimosine and its metabolites (3,4-DHP and 2,3-DHP) in leucaena when the anaerobic bacteria Synergistes jonesii (Allison et al. 1992) is absent from the rumen, may induce subclinical toxicity in grazing ruminants (Graham 2007; Dalzell et al. 2012; Phaikaew et al. 2012). There are no reports in Mexico regarding the rate of growth of cattle grazing silvopastoral systems with leucaena. The aim of the present work was to evaluate the rate of growth of cattle grazing an association of Panicum maximum and leucaena compared to that of cattle fed a high grain ration (feedlot)

Urinary Excretion of Mimosine Metabolites by Hair Sheep Fed Foliage of \u3cem\u3eLeucaena leucocephala\u3c/em\u3e

Leucaena leucocephala is an adapted legume widely distributed in the tropical regions of Mexico. The high crude protein content of leucaena leaves renders it appropriate for ruminant feeding under commercial conditions. However, the foliage contains the non-protein amino acid mimosine, which, if consumed in high amounts, may induce toxicity in animals which have not previously consumed the legume or without microorganisms capable of degrading mimosine and its derivatives 2,3-DHP (dihydroxypyridine) and 3,4-DHP (Hammond 1995, Palmer et al. 2010, Dalzell et al. 2012). Barros-Rodríguez et al. (2012) found that dry matter intake and weight gain were reduced when sheep grazed paddocks with 55,000 plants of leucaena per hectare. Early work in Australia led to the isolation of Synergistes jonesii, an anaerobic bacterium able to degrade 3,4-DHP and 2,3-DHP to non-toxic compounds (Allison et al. 1992). In Mexico, the presence of this microorganism in the rumen has not yet been confirmed. Inoculation of non-accustomed animals with rumen liquor of ruminants adapted to the consumption of leucaena can reduce the impact of mimosine and its metabolites on animal health (Ghosh et al. 2009; Palmer et al. 2010). The aim of the present work was to evaluate the effects of transferring rumen liquor of cows adapted to the consumption of L. leucocephala to sheep without experience of consumption, on urinary excretion of 3.4-DHP and 2.3-DHP by means of a colorimetric technique

Brúquidos (Coleoptera: Bruchidae) del estado de Morelos, México

Se presenta un listado faunístico de las especies de Bruchidae y de sus plantas hospederas para el estado de Morelos. Se registraron 125 especies de brúquidos, distribuidos en 19 géneros, en donde el género Acanthoscelides presentó el mayor número de especies con 48, seguido de los géneros Merobruchus, Sennius y Amblycerus con 10 especies cada uno, y Zabrotes con 9 especies. En cuanto a las plantas hospederas se identificaron 73 especies, la familia Leguminosae presentó el mayor número con 58 plantas hospederas; la familia Convolvulaceae ocupó el segundo lugar con 8 especies. Las siguientes especies de plantas constituyeron nuevos registros de hospederos: Acacia mammifera Schltdl, Albizia adinocephala (Donn. SM.) BR. & Rose, Albizia guachapele (Kunth) Dugan, Bauhinia variegata L., Heliocarpus pallidus Rose, Galactia striata (Jacq.) Urb. Mimosa benthamii J.F. Macbr, Mimosa leptocarpa Rose, Mimosa orthocarpa Spruce ex Benth., Senna holwayana (Rose) H.S. Irwin & Barneby. En relación a la biodiversidad de este grupo, con la información generada en este trabajo, Morelos actualmente representa el segundo lugar en biodiversidad nacional de este grupo, con un 37.12%; el primer lugar lo ocupa Oaxaca con 47.30%

Emisión de metano en ovinos alimentados con Pennisetum purpureum y árboles que contienen taninos condensados

El objetivo fue evaluar el efecto de los taninos condensados (TC) contenidos en el follaje de arbóreas tropicales, sobre el consumo de materia seca y orgánica (CMS, CMO), la digestibilidad de la materia seca (DMS) y emisiones de metano (CH4) en ovinos alimentados con una ración basal de pasto Pennisetum purpureum. Cuatro ovinos de pelo con un peso vivo promedio de 21.6±2.0 kg se sometieron a cuatro tratamientos en un diseño cuadro latino 4 x 4. Los tratamientos fueron P. purpureum (PP), P. purpureum + Havardia albicans (PPHA), P. purpureum + Bursera simaruba (PPBS), y P. purpureum + Acacia pennatula (PPAP); el follaje de las arbóreas se incluyó en 300 g/kg de MS de la ración. El consumo, la digestibilidad y la producción total de metano entérico se midieron por periodos de 23 h. La producción de metano se midió en cajas de respiración de circuito abierto. El consumo y digestibilidad de la MS y materia orgánica (MO) entre los tratamientos PP, PPHA, PPBS y PPAP no se afectaron por la inclusión de los follajes de arbóreas en la ración (P>0.05). Cuando la producción de CH4 se expresó en L/kg del CMS, CMO o consumo de fibra detergente neutro los resultados fueron similares entre tratamientos (PP, PPHA, PPBS y PPAP) (P>0.05). Se concluye que los TC contenidos en el follaje de Havardia albicans, Acacia pennatula y Bursera simaruba no afectaron las emisiones de CH4 al nivel de incorporación de 30 % de la MS; tampoco se observaron efectos en el CMS, CMO, DMS y concentración molar de ácidos grasos volátiles

Global investments in pandemic preparedness and COVID-19: development assistance and domestic spending on health between 1990 and 2026

Background The COVID-19 pandemic highlighted gaps in health surveillance systems, disease prevention, and treatment globally. Among the many factors that might have led to these gaps is the issue of the financing of national health systems, especially in low-income and middle-income countries (LMICs), as well as a robust global system for pandemic preparedness. We aimed to provide a comparative assessment of global health spending at the onset of the pandemic; characterise the amount of development assistance for pandemic preparedness and response disbursed in the first 2 years of the COVID-19 pandemic; and examine expectations for future health spending and put into context the expected need for investment in pandemic preparedness. Methods In this analysis of global health spending between 1990 and 2021, and prediction from 2021 to 2026, we estimated four sources of health spending: development assistance for health (DAH), government spending, out-of-pocket spending, and prepaid private spending across 204 countries and territories. We used the Organisation for Economic Co-operation and Development (OECD)'s Creditor Reporting System (CRS) and the WHO Global Health Expenditure Database (GHED) to estimate spending. We estimated development assistance for general health, COVID-19 response, and pandemic preparedness and response using a keyword search. Health spending estimates were combined with estimates of resources needed for pandemic prevention and preparedness to analyse future health spending patterns, relative to need. Findings In 2019, at the onset of the COVID-19 pandemic, US$9·2 trillion (95$7·3 trillion (95% UI 7·2–7·4) in 2019; 293·7 times the $24·8 billion (95$43·1 billion in development assistance was provided to maintain or improve health. The pandemic led to an unprecedented increase in development assistance targeted towards health; in 2020 and 2021, $1·8 billion in DAH contributions was provided towards pandemic preparedness in LMICs, and$37·8 billion was provided for the health-related COVID-19 response. Although the support for pandemic preparedness is 12·2% of the recommended target by the High-Level Independent Panel (HLIP), the support provided for the health-related COVID-19 response is 252·2% of the recommended target. Additionally, projected spending estimates suggest that between 2022 and 2026, governments in 17 (95% UI 11–21) of the 137 LMICs will observe an increase in national government health spending equivalent to an addition of 1% of GDP, as recommended by the HLIP. Interpretation There was an unprecedented scale-up in DAH in 2020 and 2021. We have a unique opportunity at this time to sustain funding for crucial global health functions, including pandemic preparedness. However, historical patterns of underfunding of pandemic preparedness suggest that deliberate effort must be made to ensure funding is maintained

Global investments in pandemic preparedness and COVID-19: development assistance and domestic spending on health between 1990 and 2026

Background The COVID-19 pandemic highlighted gaps in health surveillance systems, disease prevention, and treatment globally. Among the many factors that might have led to these gaps is the issue of the financing of national health systems, especially in low-income and middle-income countries (LMICs), as well as a robust global system for pandemic preparedness. We aimed to provide a comparative assessment of global health spending at the onset of the pandemic; characterise the amount of development assistance for pandemic preparedness and response disbursed in the first 2 years of the COVID-19 pandemic; and examine expectations for future health spending and put into context the expected need for investment in pandemic preparedness. Methods In this analysis of global health spending between 1990 and 2021, and prediction from 2021 to 2026, we estimated four sources of health spending: development assistance for health (DAH), government spending, out-of-pocket spending, and prepaid private spending across 204 countries and territories. We used the Organisation for Economic Co-operation and Development (OECD)'s Creditor Reporting System (CRS) and the WHO Global Health Expenditure Database (GHED) to estimate spending. We estimated development assistance for general health, COVID-19 response, and pandemic preparedness and response using a keyword search. Health spending estimates were combined with estimates of resources needed for pandemic prevention and preparedness to analyse future health spending patterns, relative to need. Findings In 2019, at the onset of the COVID-19 pandemic, US$9·2 trillion (95$7·3 trillion (95% UI 7·2–7·4) in 2019; 293·7 times the $24·8 billion (95$43·1 billion in development assistance was provided to maintain or improve health. The pandemic led to an unprecedented increase in development assistance targeted towards health; in 2020 and 2021, $1·8 billion in DAH contributions was provided towards pandemic preparedness in LMICs, and$37·8 billion was provided for the health-related COVID-19 response. Although the support for pandemic preparedness is 12·2% of the recommended target by the High-Level Independent Panel (HLIP), the support provided for the health-related COVID-19 response is 252·2% of the recommended target. Additionally, projected spending estimates suggest that between 2022 and 2026, governments in 17 (95% UI 11–21) of the 137 LMICs will observe an increase in national government health spending equivalent to an addition of 1% of GDP, as recommended by the HLIP. Interpretation There was an unprecedented scale-up in DAH in 2020 and 2021. We have a unique opportunity at this time to sustain funding for crucial global health functions, including pandemic preparedness. However, historical patterns of underfunding of pandemic preparedness suggest that deliberate effort must be made to ensure funding is maintained

El daño de Chaetophloeus mexicanus (Curculionidae: Scolytinae) a tallos de Eysenhardtia polystachya (Fabaceae)

Damage caused to Eysenhardtia polystachya by the bark beetle Chaetophloeus mexicanus (Coleoptera: Curculionidae; Scolytinae) was investigated as was host response to infestation. A general wood and bark anatomy of E. polystachya is given. Larvae and adults of C. mexicanus penetrate, settle down and consume noncollapsed phloem cells, vascular cambium, and secondary xylem. As a response to damage, there is a deposition of dark-staining contents (tannins) in the cells that limit the cavern. At xylem, this deposition occurs in the lumen of some vessels and fibers, but tissue proliferation did not appear. In the noncollapsed phloem a greater proportion of thick-walled cells and darkstaining contents were observed. However, above of this region, the differentiation of some parenchyma phloematic cells starts. Damage is mainly centered in the noncollapsed phloem, vascular cambium, and the just differentiated xylem cells clearly interrupting water and sap movement.Se describe el daño causado a la planta huésped (Eysenhardtia polystachya) por el descortezador Chaetophloeus mexicanus (Coleoptera: Curculionidae; Scolytinae) y la respuesta de la planta huésped a la infestación. Además se presenta una descripción de la corteza y madera de E. polystachya. Larvas y adultos de C. mexicanus penetran, se establecen y consumen células de la corteza, cámbium vascular y madera. Como respuesta al daño, hay acumulación de taninos en las células que limitan la caverna. A nivel de xilema secundario esta deposición se da en los lúmenes de algunos vasos y fibras, pero no se presentó proliferación de tejido. En el floema no colapsado se observó una mayor proporción de células con paredes engrosadas y de taninos. Sin embargo, por arriba de esta zona se inicia la diferenciación en algunas células del parénquima floemático. El daño se centra principalmente en la región del floema no colapsado, el cámbium vascular y la porción recién formada de xilema, lo que probablemente interrumpe el movimiento tanto de agua como de fotosintatos

Los crisomelinos (Coleoptera: Chrysomelidae: Chrysomelinae) del estado de Morelos

We describe some biological aspects about the Subfamily Chrysomelinae (common name catarinas) in the state of Morelos, Mexico. A total of 47 species within 8 genera and2 sub-tribes are recorded. The genus Leptinotarsa is the most species rich. Additinal information on host plants, distributions,and feeding habits is provided.En este estudio se presentan algunos aspectos sobre la biología de la subfamilia Chrysomelinae, comúnmente conocidas como catarinas. La diversidad de especies conocidas hasta el momento para el Estado de Morelos es de 47 especies incluidas en ocho géneros y dos subtribus. El género Leptinotarsa destaca por su mayor número de especies. También se incluye información adicional sobre las especies de plantas hospederas, distribución y hábitos de alimentación