66 research outputs found

    Prescribed fires

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    Fire is a natural disturbance phenomenon. Despite recognition of the importance of fire in ecosystems, fire suppression policies have been favoured, contributing to the accumulation of fuel in wildlands. Political options coupled with land abandonment, livestock reduction, plantation of monospecific species and the increasing number and length of summer droughts, as a consequence of climate change, are responsible for the occurrence of severe wildfires such as occurred in 2017 in Portugal and California. These kinds of fires have tremendous and unwanted impacts on the environment, society and the economy, including ecosystem services degradation and the loss of life (Nadal-Romero et al., 2018; Pereira et al., 2016a, Pereira et al., 2018). To tackle this problem, more investments are needed in preventive measures such as forest management techniques to reduce the amount of biomass in wildland environments. The most commonly used are mechanical thinning (e.g. clearcutting, partial cutting) and, if authorized by government bodies, prescribed fires ..

    Spatial models for monitoring the spatio-temporal evolution of ashes after fire-a case study of a burnt grassland in Lithuania

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    Ash thickness is a key variable in the protection of soil against erosion agents after planned and unplanned fires. Ash thickness measurements were conducted along two transects (flat and sloping areas) following a grided experimental design. In order to interpolate data with accuracy and identify the techniques with the least bias, several interpolation methods were tested in the grided plot. Overall, the fire had a low severity. However, the fire significantly reduced the ground cover, especially on sloping areas, owing to the higher fire severity and/or less biomass previous to the fire. Ash thickness depended on fire severity and was thin where fire severity was higher and thicker in lower fire severity sites. The ash thickness decreased with time after the fire. Between 4 and 16 days after the fire, ash was transported by wind. The greatest reduction took place between 16 and 34 days after the fire as a result of rainfall, and was more efficient where fire severity was higher. Between 34 and 45 days after the fire, no significant differences in ash thickness were identified among ash colours and only traces of the ash layer remained. The omni-directional experimental variograms showed that variable structure did not change significantly with time. The ash spatial variability increased with time, particularly on the slope, as a result of water erosion

    Short-term changes in soil Munsell colour value, organic matter content and soil water repellency after a spring grassland fire in Lithuania

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    Fire is a natural phenomenon with important implications on soil properties. The degree of this impact depends upon fire severity, the ecosystem affected, topography of the burned area and post-fire meteorological conditions. The study of fire effects on soil properties is fundamental to understand the impacts of this disturbance on ecosystems. The aim of this work was to study the short-term effects immediately after the fire (IAF), 2, 5, 7 and 9 months after a low-severity spring boreal grassland fire on soil colour value (assessed with the Munsell colour chart), soil organic matter content (SOM) and soil water repellency (SWR) in Lithuania. Four days after the fire a 400 m2 plot was delineated in an unburned and burned area with the same topographical characteristics. Soil samples were collected at 0–5 cm depth in a 20 m × 20 m grid, with 5 m space between sampling points. In each plot 25 samples were collected (50 each sampling date) for a total of 250 samples for the whole study. SWR was assessed in fine earth (< 2 mm) and sieve fractions of 2–1, 1–0.5, 0.5–0.25 and < 0.25 mm from the 250 soil samples using the water drop penetration time (WDPT) method. The results showed that significant differences were only identified in the burned area. Fire darkened the soil significantly during the entire study period due to the incorporation of ash/charcoal into the topsoil (significant differences were found among plots for all sampling dates). SOM was only significantly different among samples from the unburned area. The comparison between plots revealed that SOM was significantly higher in the first 2 months after the fire in the burned plot, compared to the unburned plot. SWR of the fine earth was significantly different in the burned and unburned plot among all sampling dates. SWR was significantly more severe only IAF and 2 months after the fire. In the unburned area SWR was significantly higher IAF, 2, 5 and 7 months later after than 9 months later. The comparison between plots showed that SWR was more severe in the burned plot during the first 2 months after the fire in relation to the unburned plot. Considering the different sieve fractions studied, in the burned plot SWR was significantly more severe in the first 7 months after the fire in the coarser fractions (2–1 and 1–0.5 mm) and 9 months after in the finer fractions (0.5–0.25 and < 0.25 mm). In relation to the unburned plot, SWR was significantly more severe in the size fractions 2–1 and < 0.25 mm, IAF, 5 and 7 months after the fire than 2 and 9 months later. In the 1–0.5- and 0.5–0.25 mm-size fractions, SWR was significantly higher IAF, 2, 5 and 7 months after the fire than in the last sampling date. Significant differences in SWR were observed among the different sieve fractions in each plot, with exception of 2 and 9 months after the fire in the unburned plot. In most cases the finer fraction (< 0.25 mm) was more water repellent than the others. The comparison between plots for each sieve fraction showed significant differences in all cases IAF, 2 and 5 months after the fire. Seven months after the fire significant differences were only observed in the finer fractions (0.5–0.25 and < 0.25 mm) and after 9 months no significant differences were identified. The correlations between soil Munsell colour value and SOM were negatively significant in the burned and unburned areas. The correlations between Munsell colour value and SWR were only significant in the burned plot IAF, 2 and 7 months after the fire. In the case of the correlations between SOM and SWR, significant differences were only identified IAF and 2 months after the fire. The partial correlations (controlling for the effect of SOM) revealed that SOM had an important influence on the correlation between soil Munsell colour value and SWR in the burned plot IAF, 2 and 7 months after the fire.info:eu-repo/semantics/publishedVersio

    The evolution of genomic imprinting:Theories, predictions and empirical tests

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    The epigenetic phenomenon of genomic imprinting has motivated the development of numerous theories for its evolutionary origins and genomic distribution. In this review, we examine the three theories that have best withstood theoretical and empirical scrutiny. These are: Haig and colleagues’ kinship theory; Day and Bonduriansky’s sexual antagonism theory; and Wolf and Hager’s maternal–offspring coadaptation theory. These theories have fundamentally different perspectives on the adaptive significance of imprinting. The kinship theory views imprinting as a mechanism to change gene dosage, with imprinting evolving because of the differential effect that gene dosage has on the fitness of matrilineal and patrilineal relatives. The sexual antagonism and maternal–offspring coadaptation theories view genomic imprinting as a mechanism to modify the resemblance of an individual to its two parents, with imprinting evolving to increase the probability of expressing the fitter of the two alleles at a locus. In an effort to stimulate further empirical work on the topic, we carefully detail the logic and assumptions of all three theories, clarify the specific predictions of each and suggest tests to discriminate between these alternative theories for why particular genes are imprinted

    The potential of shifting recombination hotspots to increase genetic gain in livestock breeding

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    International audienceAbstractBackgroundThis study uses simulation to explore and quantify the potential effect of shifting recombination hotspots on genetic gain in livestock breeding programs.MethodsWe simulated three scenarios that differed in the locations of quantitative trait nucleotides (QTN) and recombination hotspots in the genome. In scenario 1, QTN were randomly distributed along the chromosomes and recombination was restricted to occur within specific genomic regions (i.e. recombination hotspots). In the other two scenarios, both QTN and recombination hotspots were located in specific regions, but differed in whether the QTN occurred outside of (scenario 2) or inside (scenario 3) recombination hotspots. We split each chromosome into 250, 500 or 1000 regions per chromosome of which 10% were recombination hotspots and/or contained QTN. The breeding program was run for 21 generations of selection, after which recombination hotspot regions were kept the same or were shifted to adjacent regions for a further 80 generations of selection. We evaluated the effect of shifting recombination hotspots on genetic gain, genetic variance and genic variance.ResultsOur results show that shifting recombination hotspots reduced the decline of genetic and genic variance by releasing standing allelic variation in the form of new allele combinations. This in turn resulted in larger increases in genetic gain. However, the benefit of shifting recombination hotspots for increased genetic gain was only observed when QTN were initially outside recombination hotspots. If QTN were initially inside recombination hotspots then shifting them decreased genetic gain.DiscussionShifting recombination hotspots to regions of the genome where recombination had not occurred for 21 generations of selection (i.e. recombination deserts) released more of the standing allelic variation available in each generation and thus increased genetic gain. However, whether and how much increase in genetic gain was achieved by shifting recombination hotspots depended on the distribution of QTN in the genome, the number of recombination hotspots and whether QTN were initially inside or outside recombination hotspots.ConclusionsOur findings show future scope for targeted modification of recombination hotspots e.g. through changes in zinc-finger motifs of the PRDM9 protein to increase genetic gain in production species

    Processes of Initiation of Motion Leading to Bedload Transport in Gravel-bed Rivers

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    [eng] Transport processes that lead to the initiation of bedload motion in gravel‐bed rivers have not yet been clarified. We report patch‐ and grain‐scale processes involved in the initiation of bedload motion in a natural gravel‐bed stream as observed through a series of video experiments. With increasing flow strength, the phases of initiation of motion that have been identified are (1) within‐patch grain instability (grain vibration, pivoting, and grain‐scale rolling), (2) within‐patch gyratory step‐and‐rest motion, and (3) general sediment motion involving downstream transport from an individual patch and the throughput of grains inherited from upstream
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