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<p>In wetlands, the water budget is traditionally quantified by measuring the hydrologic components including precipitation, evapotranspiration and surface water-groundwater inflows and outflows. However, the reliability of measurements is often questioned due to the difficulty of rigorously monitoring all components of the water budget. Quantifying the rainfall event to water table response ratio is an alternative approach with minimal need for data commonly collected in peatland studies. However, the method has been used only in a limited number of biophysical settings including different microforms, hydroclimatic and hydrogeological settings. The objectives of this study are to quantify the reactivity of the water table to precipitation for different pristine peatlands located in different hydroclimatic conditions and to provide quantitative assessments of water storage of as many peatlands as possible. To do so, site-specific hourly water table and precipitation measurements was collected from northern peatlands worldwide. In total, data from more than 30 sites were retrieved from 8 research groups. For all peatlands, water-table depths varied between 80 cm below the peat surface and 10 cm above the peat surface. The results highlight that the hydrology of all peatlands is characterized by a shift from an environment that can store water to an environment that contributes to rapid outflow, and this is a uniform feature across sites. However, for peatlands with the lowest water storage capacities, this shift occurs during relatively moderate rainfall events (40 mm) or successive small rainfall events. Blanket peat bog best embodied this type of hydrological response. For peatlands with the highest water storage capacity, this shift occurs following multiple moderate to large precipitation events (40 mm &#8211; 80 mm) and it is strongly enhanced by the shift from high to low evaporative periods. The peatlands with the highest storage capacity are raised bogs with deep water-table. These conditions are best observed in peatlands located in geographical settings with high evaporation rates. Among all the peatlands, maximum water storage capacity for given rainfall events was equal to &#8776;150 mm. These analyses also confirm that the water table rise caused by precipitation events contain sufficient information to constrain water storage variations around monitored wells peatlands for a wide array of biophysical settings.</p>
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« On n’est plus dans l’adaptation; on est dans la gestion des risques. »
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Abstract River confluences are characterized by a complex mixing zone with three‐dimensional (3D) turbulent structures which have been described as both streamwise‐oriented structures and Kelvin–Helmholtz (KH) vertical‐oriented structures. The latter are visible where there is a turbidity difference between the two tributaries, whereas the former are usually derived from mean velocity measurements or numerical simulations. Few field studies recorded turbulent velocity fluctuations at high frequency to investigate these structures, particularly at medium‐sized confluences where logistical constraints make it difficult to use devices such as acoustic doppler velocimeter (ADV). This study uses the ice cover present at the confluence of the Mitis and Neigette Rivers in Quebec (Canada) to obtain long‐duration, fixed measurements along the mixing zone. The confluence is also characterized by a marked turbidity difference which allows to investigate the mixing zone dynamics from drone imagery during ice‐free conditions. The aim of the study is to characterize and compare the flow structure in the mixing zone at a medium‐sized (~40 m) river confluence with and without an ice cover. Detailed 3D turbulent velocity measurements were taken under the ice along the mixing plane with an ADV through eight holes at around 20 positions on the vertical. For ice‐free conditions, drone imagery results indicate that large (KH) coherent structures are present, occupying up to 50% of the width of the parent channel. During winter, the ice cover affects velocity profiles by moving the highest velocities towards the centre of the profiles. Large turbulent structures are visible in both the streamwise and lateral velocity components. The strong correlation between these velocity components indicates that KH vortices are the dominating coherent structures in the mixing zone. A spatio‐temporal conceptual model is presented to illustrate the main differences on the 3D flow structure at the river confluence with and without the ice cover. © 2019 John Wiley & Sons, Ltd.
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Several top‐down and bottom‐up forces have been put forward to explain variable infestation rates of zooplankton by epibionts. Among top‐down forces, fish predation affects epibiont prevalence on zooplanktonic organisms, either by eliminating more conspicuous, heavily burdened individuals, or by reducing population size of zooplankton hosts, with consequences for substrate availability for epibionts. However, detailed experimental‐based information on the effects of top‐down forces is still lacking. Among bottom‐up forces, light can potentially control populations of photosynthetic epibionts. Therefore, both changes in light penetration in the water column and the vertical position of hosts in the water column could affect the photic conditions in which epibionts live and could thus control their population growth. We tested experimentally the hypothesis that both light limitation and fish predation affect epibiont burden on zooplankton. Moreover, we also tested the hypothesis that zooplanktivorous fish affect the prevalence and burden of the epibiotic alga Colacium sp. (Euglenida) on zooplankton not only by direct predation, but also by affecting the vertical distribution of zooplankton. We analyzed Colacium burden on two zooplankton genera that responded differently to the presence of zooplanktivorous fish by altering their daytime vertical distributions, thus exposing photosynthetic epibionts to different light conditions. Colacium burden on the two zooplankton genera was also compared between enclosures with different degrees of light limitation. Our results suggest that (1) ambient light limitation has the potential to reduce the burden of photosynthetic epibionts on zooplankton in natural conditions, and (2) zooplankton behavior (e.g., daytime refuge use to escape fish predation) can reduce the burden by exposing photosynthetic epibionts to suboptimal light conditions.
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Abstract The mean transit time (MTT) is an important descriptor of water storage and release dynamics in watersheds. Although MTT studies are numerous for many regions around the world, they are rare for prairie watersheds where seasonally cold or dry conditions require adequate methodological choices towards MTT estimation, especially regarding the handling of sparse data records and tracer selection. To examine the impact of such choices, we used timeseries of δ 18 O and δ 2 H from two contrasted years (2014 and 2015) and relied on two metrics and two modelling methods to infer MTTs in prairie watersheds. Our focus was on nested outlets with different drainage areas, geologies, and known run‐off generation mechanisms. The damping ratio and young water fraction (i.e., the fraction of streamflow with transit times lesser than 3 months) metrics, as well as the sine‐wave modelling and time‐based convolution modelling methods, were applied to year‐specific data. Results show that young water fractions and modelled MTT values were, respectively, larger and smaller in 2014, which was a wet year, compared with that in 2015. In 2014, most outlets had young water fractions larger than 0.5 and MTT values lesser than 6 months. The damping ratio, young water fraction, and sine‐wave modelling methods led to convergent conclusions about watershed water storage and release dynamics for some of the monitored sites. Contrasting results were, however, obtained when the same method was applied using δ 2 H instead of δ 18 O, due to differing evaporation fractionation, or when the time‐based convolution modelling method was used. Some methods also failed to provide any robust results during the dry year (i.e., 2015), highlighting the difficulty in inferring MTTs when data are sparse due to intermittent streamflow. This study therefore allowed the formulation of empirical recommendations for MTT estimation in prairie environments as a function of data availability and antecedent wetness conditions.