Yves T. Prairie

Sediment organic carbon burial in agriculturally eutrophic impoundments over the last century

The OC buried in these lakes originates in both autochthonous and allochthonous production. These analyses suggest that OC sequestration in moderate to large impoundments may be double the rate assumed in previous analyses. Extrapolation suggests that they may bury 4 times as much carbon (C) as the world’s oceans. The world’s farm ponds alone may bury more OC than the oceans and 33% as much as the world’s rivers deliver to the sea.

Prevalence of heterotrophy and atmospheric CO2 emissions from aquatic ecosystems

Recent, parallel developments in the study of freshwater and marine ecosystems have provided evidence that net heterotrophic systems (those in which respiratory organic matter destruction exeeds photosynthetic production) are more prevalent than hitherto believed, including most rivers, oligo- to mesotrophic lakes and some oligotrophic regions of the ocean. In parallel, these aquatic ecosystems have been shown to act as CO2 sources to the atmosphere, as expected from the heterotrophic nature of the communities they contain. The prevalence of net heterotrophic aquatic ecosystems indicates that they must receive significant inputs of organic carbon from adjacent ecosystems, assigning an important role to the lateral exchanges of carbon between land and aquatic ecosystems, between coastal and open ocean ecosystems, as well as internal redistribution within large or complex aquatic ecosystems in determining their metabolic status and the gaseous exchange with the atmosphere. The examination of the carbon budget of ecosystems requires, therefore, an integrative approach that accounts for exchanges between compartments often studied in isolation. These recent findings conform a new paradigm of the functioning of aquatic ecosystems, and the metabolic connectivity between ecosystems in the biosphere.

What’s in an EEM? Molecular Signatures Associated with Dissolved Organic Fluorescence in Boreal Canada

Dissolved organic matter (DOM) is a master variable in aquatic systems. Modern fluorescence techniques couple measurements of excitation emission matrix (EEM) spectra and parallel factor analysis (PARAFAC) to determine fluorescent DOM (FDOM) components and DOM quality. However, the molecular signatures associated with PARAFAC components are poorly defined. In the current study we characterized river water samples from boreal Québec, Canada, using EEM/PARAFAC analysis and ultrahigh resolution mass spectrometry (FTICR-MS). Spearmans correlation of FTICR-MS peak and PARAFAC component relative intensities determined the molecular families associated with 6 PARAFAC components. Molecular families associated with PARAFAC components numbered from 39 to 572 FTICR-MS derived elemental formulas. Detailed molecular properties for each of the classical humic- and protein-like FDOM components are presented. FTICR-MS formulas assigned to PARAFAC components represented 39% of the total number of formulas identified and 59% of total FTICR-MS peak intensities, and included significant numbers compounds that are highly unlikely to fluoresce. Thus, fluorescence measurements offer insight into the biogeochemical cycling of a large proportion of the DOM pool, including a broad suite of unseen molecules that apparently follow the same gradients as FDOM in the environment.

Coupling Between Rates of Bacterial Production and the Abundance of Metabolically Active Bacteria in Lakes, Enumerated Using CTC Reduction and Flow Cytometry

A bstractIn natural bacterioplankton assemblages, only a fraction of the total cell count is active, and, therefore, rates of bacterial production should be more strongly correlated to the number of active cells than to the total number of bacteria. However, this hypothesis has seldom been tested. Herein we explore the relationship between rates of bacterial production (measured as leucine uptake) and the number of active bacteria in 14 lakes in southern Québec. Active bacteria are defined as those cells capable of reducing the tetrazolium salt CTC to its fluorescent formazan; these cells were enumerated using flow cytometry. Bacterial production varied two orders of magnitude in the lakes studied, as did the number of active bacteria, whereas the total number of bacteria varied by only sixfold. The number and proportion of active bacteria were similar among lake strata, but rates of bacterial production were highest in the epilimnion and lowest in the hypolimnion. As expected, bacterial production was better correlated to the number of active cells, and bacterial growth rates calculated for active cells ranged from 0.7 to 1.8 day−1, on average threefold higher than those calculated on the basis of total bacterial abundance. Growth rates scaled to active cells were, on average, similar among lake strata and did not show any pattern along a gradient of increasing chlorophyll concentration, so there was no systematic change of bacterial growth rates with lake productivity. In contrast, growth rates scaled to the entire bacterial assemblage were positively correlated to chlorophyll, were tenfold more variable among lakes than growth rates of active cells, and showed larger differences among lake strata. Scaling bacterial production to either the total number or the number of active cells thus results in very different patterns in bacterial growth rates among aquatic systems.

Some misconceptions about the spurious correlation problem in the ecological literature

SummaryIt is a common misconception that correlations between variables that share a common term are statistically invalid. Although the idea that such relationships are wholly or partially spurious was rejected decades ago by statisticians, ecologists continue mistakenly to exclude legitimate hypotheses on this basis. Besides directing attention to the statistical literature on the subject, we briefly reconsider the problem from 3 viewpoints: first, the confusion between spurious correlation and spurious inference, second, the problem of concept familiarity and definition, with particular reference to the self-thinning rule for plants, and third, a legitimate concern with measurement error of shared variable components.

Global abundance and size distribution of streams and rivers

Abstract To better integrate lotic ecosystems into global cycles and budgets, we provide approximations of the size-distribution and areal extent of streams and rivers. One approach we used was to employ stream network theory combined with data on stream width. We also used detailed stream networks on 2 continents to estimate the fraction of continental area occupied by streams worldwide and corrected remote sensing stream inventories for unresolved small streams. Our estimates of global fluvial area are 485 000 to 662 000 km2 and are +30–300% of published appraisals. Moderately sized rivers (orders 5–9) seem to comprise the greatest global area, with less area covered by low and high order streams, while global stream length, and therefore the riparian interface, is dominated by 1st order streams. Rivers and streams are likely to cover 0.30–0.56% of the land surface and make contributions to global processes and greenhouse gas emissions that may be +20–200% greater than those implied by previous estimates.

Variability in Fire Frequency and Forest Composition in Canada'sSoutheastern Boreal Forest: A Challenge for Sustainable ForestManagement

Because some consequences of fire resemble the effects of industrial forest harvesting, forest management is often considered as a disturbance having effects similar to those of natural disturbances. Although the analogy http://www.ecologyandsociety.org/vol2/iss2/art6/ (1 of 11) [9/5/2008 10:08:21 AM] Conservation Ecology: Variability in fire frequency and forest composition i...s southeastern boreal forest: a challenge for sustainable forest management between forest management and fire disturbance in boreal ecosystems has some merit, it is important to recognize that it has limitations. First, normal forest rotations truncate the natural forest stand age distribution and eliminate over-mature forests from the landscape. Second, in the boreal mixedwoods, natural forest dynamics following fire may involve a gradual replacement of stands of intolerant broadleaf species by mixedwood and then softwood stands, whereas current silvicultural practices promote successive rotations of similarly composed stands. Third, the large fluctuations observed in fire frequency during the Holocene limit the use of a single fire cycle to characterize natural fire regimes. Short fire cycles generally described for boreal ecosystems do not appear to be universal; rather, shifts between short and long fire cycles have been observed. These shifts imply important changes in forest composition at the landscape and regional levels. All of these factors create a natural variability in forest composition that should be maintained by forest managers concerned with the conservation of biodiversity. One avenue is to develop silvicultural techniques that maintain a spectrum of forest compositions over the landscape.

Browning of Boreal Freshwaters Coupled to Carbon-Iron Interactions along the Aquatic Continuum

The color of freshwaters, often measured as absorbance, influences a number of ecosystem services including biodiversity, fish production, and drinking water quality. Many countries have recently reported on increasing trends of water color in freshwaters, for which drivers are still not fully understood. We show here with more than 58000 water samples from the boreal and hemiboreal region of Sweden and Canada that absorbance of filtered water (a420) co-varied with dissolved organic carbon (DOC) concentrations (R2 = 0.85, P<0.0001), but that a420 relative to DOC is increased by the presence of iron (Fe). We found that concentrations of Fe significantly declined with increasing water retention in the landscape, resulting in significantly lower Fe concentrations in lakes compared to running waters. The Fe loss along the aquatic continuum corresponded to a proportional loss in a420, suggesting a tight biogeochemical coupling between colored dissolved organic matter and Fe. Since water is being flushed at increasing rates due to enhanced runoff in the studied regions, diminished loss of Fe along the aquatic continuum may be one reason for observed trends in a420, and in particular in a420/DOC increases. If trends of increased Fe concentrations in freshwaters continue, water color will further increase with various effects on ecosystem services and biogeochemical cycles.

Oxic water column methanogenesis as a major component of aquatic CH4 fluxes

Methanogenesis has traditionally been assumed to occur only in anoxic environments, yet there is mounting, albeit indirect, evidence of methane (CH4) production in oxic marine and freshwaters. Here we present the first direct, ecosystem-scale demonstration of methanogenesis in oxic lake waters. This methanogenesis appears to be driven by acetoclastic production, and is closely linked to algal dynamics. We show that oxic water methanogenesis is a significant component of the overall CH4 budget in a small, shallow lake, and provide evidence that this pathway may be the main CH4 source in large, deep lakes and open oceans. Our results challenge the current global understanding of aquatic CH4 dynamics, and suggest a hitherto unestablished link between pelagic CH4 emissions and surface-water primary production. This link may be particularly sensitive to widespread and increasing human influences on aquatic ecosystem primary productivity.

Fractal dimension estimates of a fragmented landscape: sources of variability

Although often seen as a scale-independent measure, we show that the fractal dimension of the forest cover of the Cazaville Region changes with spatial scale. Sources of variability in the estimation of fractal dimensions are multiple. First, the measured phenomenon does not always show the properties of a pure fractal for all scales, but rather exhibits local self-similarity within certain scale ranges. Moreover, some sampling components such as area of sampling unit, the use of a transect in the estimation of the variability of a plane, the location, and the orientation of a transect all affect, to different degrees, the estimation of the fractal dimension. This paper assesses the relative importance of these components in the estimation of the fractal dimension of the spatial distribution of woodlots in a fragmented landscape. Results show that different sources of variability should be considered when comparing fractal dimensions from different studies or regions.