ABSTRACT
RESUMEN Kinosternon chimalhuaca (Casquito de Jalisco) es una tortuga kinosternida endémica de México. La talla máxima de longitud de caparazón (CL) es de 160 mm en machos y de 130 mm en hembras. Tiene un pequeño rango de distribución en la costa del Pacífico de Jalisco y Colima (México), desde el río Tuito en Jalisco hasta el río Cihuatlán en el noroeste de Colima. Este nuevo registro en Puerto Vallarta, Jalisco, extiende su distribución al menos 32 km al norte de la localidad más septentrional conocida. Se registra un nuevo tamaño máximo (CL) para la especie de 172,00 mm (un macho).
ABSTRACT Kinosternon chimalhuaca (Jalisco Mud Turtle) is a kinosternid turtle endemic to Mexico. The previously recorded maximun carapace length (CL) is 160 mm in males and 130 mm in females. It has a small distribution range along the Pacific coast of Jalisco and Colima, Mexico, from the rio Tuito in Jalisco to the rio Cihuatlán in northwestern Colima. This new record in Puerto Vallarta, Jalisco, extends its distribution at least 32 km north from the northernmost known locality. A new maximun size (CL) for the species of 172.00 mm (one male) is recorded.
ABSTRACT
Introducción: Aedes aegypti (L) (Diptera: Culicidae), es una especie cosmopolita y vector de arbovirosis. Las variaciones de la temperatura y salinidad del agua influyen en la eclosión y supervivencia de fases larvales. Objetivo: Evaluar el efecto de diferentes temperaturas y salinidades en la eclosión de huevos y la supervivencia de larvas, pupas y adultos bajo condiciones de laboratorio. Métodos: Se colectaron larvas de Ae. aegypti, de reservorios artificiales en la zona periurbana de Puerto Vallarta, Jalisco, México, y se mantuvieron hasta la fase adulta. Los huevos obtenidos se sometieron a ocho temperaturas (15, 17, 20, 25, 27, 30, 32 y 35 °C). Se colocaron 15 huevos por quintuplicado y se evaluó la eclosión durante 96 h. Se colocaron 100 huevos con agua ajustada a 0.3, 2, 5, 10, 15,18 y 22 ups y se evaluó la eclosión hasta las 96 h. Adicionalmente se utilizaron larvas del estadio IV, por quintuplicado, sometiéndose a las mismas salinidades y se evaluó la supervivencia hasta las 48 h. El efecto de la salinidad en la ovoposición de las hembras se llevó a cabo introduciendo recipientes con las mismas concentraciones salinas, dentro en las jaulas entomológicas. Resultados: Se registró el 100 por ciento de eclosión a las 24 y 48 h; la temperatura de 35° C no registró eclosión. Las salinidades de 22 y 18 ups, provocaron mortalidad del 100 por ciento a las 24 h. En la salinidad de 15 ups, sobrevivió el 50 por ciento. Las concentraciones de 2, 5 y 10 ups demostraron 100 por ciento de supervivencia hasta la fase de adulto. La supervivencia de larvas del estadio IV en los tratamientos 2, 5 y 10 fue del 100 por ciento y en 15,18 y 22 ups disminuyó a 50, 80 y 100 por ciento, respectivamente (p˂ 0,05). Las diferentes concentraciones salinas no afectaron significativamente la ovoposición. La eclosión solo se presentó en las concentraciones de 0,3; 2; 5 y 10 ups. Los huevos ovopositados en concentraciones de 15, 18 y 22 ups no eclosionaron hasta que fueron transferidos a agua dulce con porcentajes de eclosión de entre el 80 y 90 por ciento. Conclusiones: Los embriones de Ae. aegypti poseen una amplia plasticidad para soportar cambios drásticos de temperatura y salinidad. El control efectivo de sus poblaciones debe incluir la revisión de charcas o reservorios que contengan aguas salobres hasta 18 ups(AU)
Introduction: Aedes aegypti (L) (Diptera: Culicidae) is a cosmopolitan species and a vector of arboviruses. Variations in the temperature and salinity of the water affect eclosion and survival during the larval stages. Objective: Evaluate the effect of different temperatures and salinities on the eclosion of eggs and the survival of larvae, pupae and adults in laboratory conditions. Methods: Ae. aegypti larvae were collected from artificial reservoirs in a peri-urban area of Puerto Vallarta, Jalisco, Mexico, and maintained until the adult stage. The eggs obtained were subjected to eight temperatures (15, 17, 20, 25, 27, 30, 32 and 35 °C). Fifteen eggs were placed in quintuplicate and eclosion was evaluated for 96 h. One hundred eggs were placed with water adjusted to 0.3, 2, 5, 10, 15, 18 and 22 psu and eclosion was evaluated until 96 h. Additionally, stage IV larvae were used in quintuplicate, subjecting them to the same salinities and evaluating survival until 48 h. The effect of salinity on oviposition by females was determined by introducing containers with the same salinity into the entomological cages. Results: 100 percent eclosion was recorded at 24 and 48 h, whereas no eclosion occurred at a temperature of 35 °C. Salinities of 22 and 18 psu caused 100 percent mortality at 24 h, whereas 50 percent survived at a salinity of 15 psu. At concentrations of 2, 5 and 10 psu 100 percent of the larvae survived until the adult stage. Survival of stage IV larvae in treatments 2, 5 and 10 was 100%, whereas in 15, 18 and 22 psu it fell to 50, 80 and 100 percent, respectively (p˂ 0.05). The different salinities did not affect oviposition significantly. Eclosion only occurred at concentrations of 0.3, 2, 5 and 10 psu. Oviposited eggs at concentrations of 15, 18 and 22 psu did not eclose until they were transferred to fresh water, where eclosion percentages ranged between 80 percent and 90 percent. Conclusions: Ae. aegypti embryos have great plasticity to endure drastic changes in temperature and salinity. Effective control of their populations should include inspection of ponds and reservoirs containing brackish water of up to 18 psu(AU)
Subject(s)
Animals , Temperature , Water Microbiology , Aedes/growth & development , Larva/microbiology , Salinity , Mosquito Vectors/immunology , SurvivorshipABSTRACT
Introducción: el aumento de enfermedades transmitidas por mosquitos se ha asociado a cambios globales: el crecimiento de la población, la urbanización y el cambio climático. Dentro de las alternativas para evitar epidemias están el control químico y biológico. Objetivos: determinar las concentraciones efectivas de tres compuestos químicos para el control de larvas de Aedes aegypti en la región costa norte de Jalisco, México, y evaluar la capacidad predatoria de diversas especies acuáticas sobre larvas de mosquitos. Métodos: se evaluaron cinco concentraciones de temefos (1,5; 1; 0,1; 0,05 y 0,01 g/L), hipoclorito de sodio (5,5; 0,55; 0,05; 0,005 y 0,0005 g/L) y detergente (10; 5; 1; 0,5; 0,1 g/L). Se determinó la muerte de las larvas a 1, 3, 6 y 24 h y se calculó la CL50. Se evaluaron cuatro especies de peces, un crustáceo y una larva de díptero culícido. Se les suministraron diferentes cantidades de larvas (5, 10, 30, 50 y 80) por quintuplicado y se registró su consumo a diferentes tiempos (1, 3, 5, 9 y 24 h). Resultados: el temefos provocó el 100 por ciento de mortalidad en todas las concentraciones probadas. El NaClO provocó mortalidad del 100 por ciento en las dos concentraciones más altas. El detergente fue más eficiente a las tres concentraciones mayores. Los peces demostraron un consumo de casi el 100 por ciento en la mayoría de las densidades probadas. La larva de díptero culícido demostró un consumo cercano al 80 por ciento, el crustáceo solo consumió el 53 por ciento Conclusiones: el uso del temefos debe continuar siendo el larvicida químico de elección en Puerto Vallarta, México. La utilización de peces nativos se sugiere como adecuada para el control biológico(AU)
Introduction: the increase of diseases transmitted by mosquitoes has been associated to global changes such as the population growth, urbanization and climate change. Among the alternatives to avoid epidemics are the chemical and biological control. Objectives: to determine effective concentrations of three chemical compounds to control Aedes aegypti larvae in the northern coastal region of Jalisco and to evaluate the predatory ability of various aquatic species on mosquito larvae. Methods: five concentrations of temephos of (1.5, 1, 0.1; 0.05 and 0.01 g/L), sodium hypochlorite (5.5, 0.55, 0.05, 0,005 and 0.0005 g/L) and detergent (10, 5, 1, 0.5, 0.1 g/L) were evaluated. Larval death was estimated at different times (1, 3, 5, 9 and 24 h) and the LC50 was calculated. Four fish species, one crustacean and one dipteral culicid larva were evaluated. All were provided with different numbers of larvae (5, 10, 30, 50 and 80) five times and the larval consumption was recorded at different times (1, 3, 5, 9 and 24 h). Results: temephos caused 100 percent mortality of larvae in all tested concentrations. The NaClO caused 100 percent mortality at the two highest concentrations. The detergent was more efficient at the three higher concentrations. Fish proved to be efficient predators of larvae, as they consumed almost 100 percent of larvae in most of tested densities. The diptera culicid larva reached around 80 percent consumption whereas crustacean consumed only 53 percent. Conclusions: the use of temephos should remain the chemical larvicide of choice in Puerto Vallarta region. Native fish are suggested to be used as appropriate biological control agents(AU)
Subject(s)
Temefos , Pest Control, Biological/methods , Aedes , Larva , MexicoABSTRACT
Understanding the interplay between thermal variations and sex ratio in reptiles with temperature-dependent sex determination is the first step for developing long-term conservation strategies. In case of crocodilians, the information is fragmentary and insufficient for establishing a general framework to consider how thermal fluctuation influence sex determination under natural conditions. The main goal of this study was to analyze thermal variation in nests of Crocodylus moreletii and to discuss the potential implications for predicting offspring sex ratio. The study was carried out at the Centro de Estudios Tecnológicos del Mar N° 2 and at the Sistemas Productivos Cocodrilo, Campeche, Mexico. Data was collected in the nesting season of Morelet's Crocodiles during three consecutive seasons (2007-2009). Thermal fluctuations for multiple areas of the nest chamber were registered by data loggers. We calculate the constant temperature equivalent based on thermal profiles among nests to assess whether there are differences between the nest temperature and its equivalent to constant temperature. We observed that mean nest temperature was only different among nests, while daily thermal fluctuations vary depending on the depth position within the nest chamber, years and nests. The constant temperature equivalent was different among and within nests, but not among survey years. We observed differences between constant temperature equivalent and mean nest temperature both at the top and in the middle of the nest cavities, but were not significantly different at the bottom of nest cavities. Our results enable examine and discuss the relevance of daily thermal fluctuations to predict sex ratio of the Morelet's Crocodile.