Effects of deforestation on ecosystem carbon densities in central Saskatchewan, Canada
Introduction
After fossil fuel burning, land-use change is the next largest source of anthropogenic carbon emissions. Houghton (1999) estimated that 87% of global emissions from land-use change over the past 150 years were from agricultural expansion in forested regions. Past deforestation and associated agricultural activities reduced both vegetation biomass and soil organic matter (Houghton et al., 1983, Buringh, 1984, Schlesinger, 1984, Mann, 1986, Houghton and Skole, 1990, Davidson and Ackerman, 1993).
Peak agriculture-related deforestation in eastern North America occurred a century ago. More recently, rural depopulation, farmland abandonment and expansion of tree plantations has led to increases in the extent of forest cover in this and other temperate regions (Williams, 1989, Rudel, 1998, FAO, 2001). Land-use change in western Canada runs counter to this pattern. In central Saskatchewan, agricultural settlement was barely underway by 1900. Development of croplands and pastures persisted for the next 90 years (Ramankutty and Foley, 1999) and deforestation may not yet have subsided (Fitzsimmons, 2002a, Hobson et al., 2002).
Houghton (1999) estimates losses of 85 Mg C ha−1 for vegetation, and 51 Mg C ha−1 for the top 1 m of soil, for North American boreal regions converted to agriculture. Beyond this continental estimate, more specific data on the effects of deforestation on carbon densities for western Canada are not available. Numerous estimates are available for vegetation biomass (Sulistiyowati, 1998), soil carbon storage (Xiao, 1987, Ellert and Bettany, 1995; Pennock and van Kessel, 1997a, Pennock and van Kessel, 1997b) or both (Halliwell and Apps, 1997a, Halliwell and Apps, 1997b, Halliwell and Apps, 1997c; Gower et al., 1997) at sites within central Saskatchewan. However, these data do not facilitate direct comparisons of forest and agricultural lands because of differences in methodology and site conditions (e.g. soil type). Comparable estimates of C densities at forested and agricultural sites are necessary to assess the impact of past deforestation and future land-use change on C stocks.
We investigated ecosystem C densities for forested and deforested sites in the Boreal Plain Ecozone (Acton et al., 1998) of Saskatchewan. Deforestation is defined as “the removal of a forest stand where the land is put to a non-forest land-use” (Helms, 1998, p. 44). Deforested sites included both pastures and cultivated fields. The objectives of the study were: (i) to estimate the magnitude of C losses associated with deforestation at sites; and (ii) to partition these losses among specific ecosystem components such as above-ground vegetation and soils to a fixed depth.
Our research design was a comparative mensurative experiment (Hurlbert, 1984) using space as an analogue for time. Three treatment groups were compared with the expectation that the effects of land-use on C density would be exhibited as differences in C densities among the forest group, pasture group and cultivated group. Three hypotheses were investigated. For soil organic carbon (SOC), we hypothesized:Cultivated sites were expected to have the lowest SOC due to tillage-induced losses (see reviews by Mann (1986), and Davidson and Ackerman (1993)). For C in aboveground vegetation, we hypothesized:Forests were expected to have the greatest aboveground C because of their perennial woody tissue and taller stature. Because of fertilization and lack of grazing at cultivated sites, biomass C values were expected to exceed those at pastures. For estimated ecosystem C (aboveground vegetation plus SOC), we hypothesized:Forests were expected to have the greatest C densities because of greater aboveground vegetation C. Cultivated sites were expected to have lowest C densities due to tillage-induced SOC losses.
Section snippets
Site selection and site descriptions
The Cookson study area is located approximately 40 km north of the Town of Shellbrook, in central Saskatchewan. It is approximately 30 000 ha in size, and includes Township 53, ranges 1 (west half), 2–4 (east half), West of the 3rd Meridian. Vegetation in the study area prior to agricultural settlement was mixedwood boreal forest (Weir et al., 2000). Six sites were selected within the Cookson study area for each of three treatment groups: forests, pastures, and cultivated fields. The site number,
Soil descriptions and SOC densities
The forested sites exhibited a diverse array of soil taxa. Luvisols (Alfisols), Brunisols (Inceptisols), Chernozems (Mollisols), and Gleysols (equivalent to the Aquic suborder of the USDA soil orders above) were each the dominant soil order at one or more individual forest sites. Luvisolic and Chernozemic soils were dominant at all pasture sites. Gleysols occurred at only two pastures and Brunisols were entirely absent. Chernozems were the most frequently occurring soil order at five of six
Discussion
A basic assumption for this comparative mensurative experiment is that the three groups of sites were similar prior to the imposition of land-use differences. Site selection was used to minimize ecological differences among the three treatment groups. All sites were located in a relatively small geographic area (three townships) to minimize variation in historic climate and vegetation. Soil maps were used to restrict sampling sites to a limited range of landforms and dominant soil taxa.
Conclusions and management implications
Assessing the impact of deforestation and cultivation on SOC in this region will require long-term manipulative experiments or other research methodologies free from the confounding effects of inherent spatial variability in SOC densities among sites. The influence of groundwater on SOC in this region is worthy of further investigation. Localized upland areas with shallow depths to groundwater may hold a disproportionately large share of the total SOC stocks that exist across a regional
Acknowledgements
This research was supported by the Centre for Studies in Agriculture, Law and Environment, the Department of Soil Science and the Department of Plant Sciences at the University of Saskatchewan. In-kind support was provided by Parks Canada and the Saskatchewan Research Council. Michael Solohub, Masae Takeda, Colleen Watson, Randy Olson and numerous others provided valuable field and lab assistance. The research would not have been possible without the support of land owners and land managers
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