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Long Incubation Periods (long + incubation_period)
Selected AbstractsEvolutionary innovations of squamate reproductive and developmental biology in the family ChamaeleonidaeBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2010ROBIN M. ANDREWS The availability of molecular phylogenies has greatly accelerated our understanding of evolutionary innovations in the context of their origin and rate of evolution. Here, we assess the evolution of reproductive mode, developmental rate and body size in a group of squamate reptiles: the chameleons. Oviparity is ancestral and viviparity has evolved at least twice: Bradypodion and members of the Trioceros bitaeniatus clade are viviparous. Viviparous species are medium-sized as a result of convergence from either small-sized ancestors or large-sized ancestors, respectively, but do not differ from oviparous species in clutch size, hatchling size or the trade-off between clutch and hatchling size. Basal chameleons (Brookesia, Rhampholeon and Rieppeleon) are small-sized and have developmental rates comparable with those of other lizards. Derived chameleons (Calumma, Chamaeleo, Trioceros and Furcifer) are mostly large-sized and all have relatively slow developmental rates. Several clades of derived chameleons also exhibit developmental arrest (embryonic diapause or embryonic diapause plus cold torpor) and incubation periods extend to 6,10 months or more. Developmental arrest is associated with dry, highly seasonal climates in which the period favourable for oviposition and hatching is short. Long incubation periods thus ensure that hatching occurs during the favourable season following egg laying. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 656,668. [source] Primary cutaneous actinomycosis of the elbow with an exceptionally long incubation periodINTERNATIONAL JOURNAL OF DERMATOLOGY, Issue 3 2008Ghaninejad Hayedeh MD No abstract is available for this article. [source] Longitudinal study of the spread of ovine Johne's disease in a sheep flock in southeastern New South WalesAUSTRALIAN VETERINARY JOURNAL, Issue 4 2005L RAST Objective The aim of this study was to apply whole flock testing over time to determine the prevalence, distribution and spread of infection in a recently infected flock, with a view to planning intervention strategies for disease control. Procedure Serology, pooled faecal culture (PFC) and histology were used to determine the distribution and persistence of infection in a sheep flock in south east New South Wales between 1997 and 2002. Partial flock testing was done up to June 2000, after which annual whole flock testing, using PFC was performed. Results Faecal shedding of M a paratuberculosis was not detected in home-bred sheep until 7 years after the introduction of infected sheep in 1993. For at least 7 years there was clustering of infection and shedding within two age groups only. The infected groups appeared to have been exposed to infection (mycobacterial contamination) at an early age (< 12 months) and commenced shedding at 5 years of age or older. Groups that were exposed to contamination as adults did not shed detectable amounts of M a paratuberculosis during the study period. Conclusion Clustering of detectable infection in age groups of sheep that were exposed as lambs was a feature on this farm, providing indirect evidence of finite duration of survival of M a paratuberculosis on pasture and the influence of age on the susceptibility of sheep to develop detectable M a paratuberculosis infection. Spread of infection occurred very slowly and was probably related to the long incubation period (exposure to shedding interval) of 5 years observed on this farm. The findings suggest that partial flock culling, selective grazing management and vaccination could lead to a reduction in mycobacterial contamination on farm to a level at which patent infection no longer occurs. Better understanding of disease spread within flocks over time through flock profiling using PFC will help in devising surveillance strategies (including testing protocols for market assurance testing) to detect infected flocks where there has been clustering and slow spread of infection. [source] Breeding biology of White-rumped Tanagers in central BrazilJOURNAL OF FIELD ORNITHOLOGY, Issue 3 2010Luane R. Dos Santos ABSTRACT White-rumped Tanagers (Cypsnagra hirundinacea) are widely distributed in northern Brazil, Bolivia, and Paraguay, and are classified as vulnerable in the state of Paraná and as endangered in the state of São Paulo, Brazil. Little is currently known about their breeding biology. We studied the breeding behavior of White-rumped Tanagers in the Cerrado (Neotropical savanna) in central Brazil from 2002 to 2007. The breeding period extended from mid-August to mid-December. Nests were cup-shaped and located mainly in trees of the genus Kielmeyera at a mean height of 3.7 ± 0.3 m (SE). Clutch sizes varied from one to three eggs and the incubation period lasted an average of 16.0 ± 0.3 d. Incubation was by females only and started with the laying of the first egg. Mean nest attentiveness (percent time on nests by females) was 64 ± 0.08%. Nestlings were fed by males, females, and, when present, helpers. The mean rate of food delivery rate to nests was 5.2 ± 0.4 items/h, with rates similar for males (mean = 2.7 ± 0.3 items/h) and females (mean = 2.4 ± 0.3 items/h). The mean duration of the nestling period was 12.1 ± 0.5 d. Compared to many temperate species of tanagers, White-rumped Tanagers in our study had relatively small clutches, low nest attentiveness, and long incubation periods. As with other tropical species, such characteristics might be due to food limitation or high rates of nest predation. RESUMEN Cypsnagra hirundinacea está ampliamente distribuida desde el norte de Brasil, Bolivia y Paraguay, y está clasificada como vulnerable en el estado de Paraná y en peligro en el estado de São Paulo, Brasil. Actualmente poco es conocido sobre su biología reproductiva. Estudiamos el comportamiento reproductivo de C. hirundinacea en el cerrado (Sabana Neotropical) en la región central de Brasil desde el 2002 hasta el 2007. El periodo reproductivo se extiende desde mediados de agosto hasta mediados de diciembre. Los nidos en forma de copa estaban localizados principalmente en arboles del genero Kielmeyera a una altura promedio de 3.7 ± 0.3 (ES) m. El tamaño de la nidada vario entre uno y tres huevos y el periodo de incubación duro en promedio 16 ± 0.3 días. La incubación fue realizada exclusivamente por la hembra y comenzó después de la puesta del primer huevo. El promedio de atención al nido (porcentaje del tiempo en el nido por parte de la hembra) fue de 64 ± 0.08%. Los polluelos fueron alimentados por el macho, la hembra y, cuando estaban presentes, ayudantes. El promedio de la tasa de alimentación al nido fue de 5.2 ± 0.4 viajes/hr, con tasas similares entre el macho (promedio = 2.7 ± 0.3 viajes/hr) y la hembra (promedio = 2.4 ± 0.3 viajes/hr). El promedio de duración del periodo de polluelos fue de 12.1 ± 0.5 días. Comparado con muchas especies de tangaras de la zona temperada, C. hirundinacea tiene una nidada relativamente pequeña, baja atención al nido y un periodo largo de incubación. Pero las diferencias con otras especies tropicales en estas variables se pueden deber a variación en la disponibilidad de alimento o altas tasa de depredación. [source] Antifungal susceptibility testing by flow cytometry: is it the future?MYCOSES, Issue 4 2006Luís André Vale-Silva Summary The current increase in the number and significance of fungal infections, the expanding armamentarium of antifungal agents, and the emergence of the problem of antifungal drug resistance have been intensifying the importance of antifungal susceptibility testing (AST). The Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) in the United States and the Antifungal Susceptibility Testing Subcommittee of the European Committee on Antimicrobial Susceptibility Testing (AFST-EUCAST) published standard methodologies in order to achieve higher reproducibility and allow direct inter-laboratory comparison of the susceptibility results. Nevertheless, several problems remain unresolved and the methods depend on long incubation periods of a minimum of 24 h (EUCAST) or even 48 h (CLSI). Over the last 15 years, successful applications of flow cytometric techniques to AST of both yeast and moulds have been reported. These techniques are based on the analysis of a great number of fungal cells individually and frequently rely on short incubation times of no more than a few hours. Considering these attributes, flow cytometry (FC) seems to have the potential to achieve clinical usefulness in the near future. The collection of data on the reproducibility of the results and on the correlation with clinical outcomes has barely started, however. Practical validation of the experimental methodologies is not granted before a significant amount of data addressing those questions is available. [source] A 15N-aided artificial atmosphere gas flow technique for online determination of soil N2 release using the zeolite Köstrolith SX6®RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 22 2006Oliver Spott N2 is one of the major gaseous nitrogen compounds released by soils due to N-transformation processes. Since it is also the major constituent of the earth's atmosphere (78.08% vol.), the determination of soil N2 release is still one of the main methodological challenges with respect to a complete evaluation of the gaseous N-loss of soils. Commonly used approaches are based either on a C2H2 inhibition technique, an artificial atmosphere or a 15N-tracer technique, and are designed either as closed systems (non-steady state) or gas flow systems (steady state). The intention of this work has been to upgrade the current gas flow technique using an artificial atmosphere for a 15N-aided determination of the soil N2 release simultaneously with N2O. A 15N-aided artificial atmosphere gas flow approach has been developed, which allows a simultaneous online determination of N2 as well as N2O fluxes from an open soil system (steady state). Fluxes of both gases can be determined continuously over long incubation periods and with high sampling frequency. The N2 selective molecular sieve Köstrolith SX6® was tested successfully for the first time for dinitrogen collection. The presented paper mainly focuses on N2 flux determination. For validation purposes soil aggregates of a Haplic Phaeozem were incubated under aerobic (21 and 6 vol.% O2) and anaerobic conditions. Significant amounts of N2 were released only during anaerobic incubation (0.4 and 640.2,pmol N2 h,1,g,1 dry soil). However, some N2 formation also occurred during aerobic incubation. It was also found that, during ongoing denitrification, introduced [NO3], will be more strongly delivered to microorganisms than the original soil [NO3],. Copyright © 2006 John Wiley & Sons, Ltd. [source] | |||||||||||||