Approximately 4 Pg C yr-1 (1 Pg = 1015 grams) are released into the atmosphere during the burning of biomass. While most of this carbon is reaccumulated in plant biomass through vegetation regrowth on the fire-disturbed areas, in tropical regions Houghton (1991) estimates there is a net release of ~0.7 Pg C yr-1 to the atmosphere due to burning of biomass in cleared forest lands. When considering biomass burning on a global scale, researchers have discounted the role of fire in boreal forests (see, e.g., Seiler and Crutzen, 1980). However, several oversights were made in these earlier studies. First, the total area burned in boreal forests was significantly underestimated, by as much as an order of magnitude. Second, these initial studies focused on the burning of aboveground biomass, ignoring the large amounts of organic matter in the ground layer that are consumed during fires in boreal forests. Studies have indicated that fires in boreal forests could become a significant source of carbon to the atmosphere over the next half century (Kasischke et. al. 1994a).
Several researchers have demonstrated that low resolution (1 to 4 km)
satellite imagery from NOAA's AVHRR system can be used to map and locate
fires in Russian and Alaskan boreal forests (Cahoon et. al., 1994;
Kasischke et. al., 1993; Kasischke and French, 1994; French
et. al. 1994). In this paper, we develop a ground-based model
of biomass levels and carbon-release during fires in Alaskan boreal forests
to estimate the amounts of carbon released during fire in this region for
1990 and 1991.
The potential vegetation map of Kuchler (1970) was digitized and entered into a geographic information system to define the boreal forest region of Alaska. Using the approach of Gabriel and Tande (1983), the physiographic divisions defined by Wahrhaftig (1965) were used to create different boreal forest regions. A digitized version of Wahrhaftig's classification was obtained from the U.S. Geological Survey, and imported into the GIS. By merging Wahrhaftig's and Kuchler's data sets, 64 distinct forest regions were created within the boreal zone of Alaska.
Much of the land area within the boreal forest zone of Alaska is not covered by forest (e.g., rivers and streams, lakes and ponds, non-forested peatlands, sub-alpine tundra, alpine tundra, non-vegetated, rocky surfaces, areas cleared for agricultural purposes, and urban areas). 1° x 3° U.S. Geological Survey topographic maps were used to estimate the non-forested area. The percent areal coverage (to within 5%) was estimated for three different land cover categories for each region: non-vegetated, including water,- glacier and rock covered (areas above 2500 m in elevation usually are devoid of vegetation cover in Alaska); vegetated areas above the beeline (above 1000 m); and wetlands. The remaining area was assumed to be covered by forests. Based upon this approach, it was determined that 50.5 % of Alaska's boreal forest zone is covered by forest (28.5 x 106 ha), 18.3% by peatlands (10.3 x 106 ha), 6.8 by alpine and sub-alpine tundra (3.9 x 106 ha), and 24.3% by non-vegetated surfaces (13.7 x 106 ha).
The approach of Seiler and Crutzen (1980) was used to estimate
carbon released (Cr) from wildfires in Alaska:
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(1)
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To estimate the amounts of carbon released during fires in the Alaskan boreal forests, the following assumptions were made: (1) the boreal forest is comprised of several different forest types each having different rates of biomass accumulation as a function of stand age; (2) fire frequency is a primary determinant of stand age distribution in boreal forests, and determines the average levels of biomass present; and (3) the amount of biomass consumed during fires is dependent on forest type. To develop biomass estimates for the different boreal forest regions, the following assumptions were used
1. The majority of forest succession in Alaska occurs after disturbance by fire;
2. The boreal forests of Alaska are divided into two forest types,: following Van Cleve et al. (1983). The first forest type consists of a single-species chronosequence, where the dominant canopy trees are black spruce or white spruce. The second forest type follows a chronosequence where a disturbed site is first populated by balsam poplar, trembling aspen, or paper birch. These deciduous species are then succeeded by white spruce
3. The percentage of the landscape occupied by these two forest types is constant throughout the state; and
4. The maximum level of biomass accumulation as a function of time after disturbance is constant.
Based on Yarie (1983) we estimate forest type I comprises 60% of Alaska's boreal forest and forest type 11 comprises the remaining 40%. The maximum biomass levels are 6 kg-m-2 for forest type I (after 150 yrs) and 18 kg-m-2 for forest type 11 (after 250 yrs) (Yarie 1983; Van Cleve et. al. 1983). For both forest types, after maximum biomass is reached, the forests become overmature and begin to gradually lose biomass because of mortality of overstory trees. Several factors determine the pattern of biomass accumulation in the ground layer. Cold soils and short growing seasons in boreal forests lead to very low rates of decomposition and accumulation of large amounts of dead-organic matter in the ground layer. Because forest type I is found in areas of lower average soil temperatures (including areas underlain by permafrost) than forest type II, the decomposition rates in these sites are lower, leading higher levels of ground-layer biomass. Fire results in a dramatic increase ID both ground-layer temperatures and rates of decomposition (Viereck, 1983), which leads to the net loss of carbon from the ground layer for the first several years after a fire. Finally, not all ground-layer biomass is consumed during a fire. Measurements by Kasischke a al. (1994b) show that 37% of the total ground-layer biomass was consumed during a fire in a site similar to forest type 1, while in a site similar to forest type 11, 70% of the ground layer biomass was consumed during a fire.
The levels of below-ground biomass for the two different forest types were estimated using data from Van Cleve et al. (19833 and Yarie (1983). The levels at a stand age of 200 years after a fire were assumed to be 20 kg-m-2 for forest type I and 10 kg-m-2 for forest type 11. Figure 1 presents the patterns of. biomass accumulation for the two forest types.
Yarie (1981) has shown that where fire is the dominant disturbance factor,
the stand-age distribution in boreal forests can be determined by the fire
frequency (f). Using a Weibel distribution, the stand age distribution,
p(t), can be calculated as:
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(2)
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Given p(t) and the pattern of biomass accumulation as function
of time [B(t)], the average level of biomass stored [Ba]
can be estimated as
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(3)
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To determine the fire frequency for each region used in this' study, data on the locations and sizes of all fires in Alaska since 1954 were obtained (Barry, 1993). his information was imported into the GIS data base, and fire frequency was estimated for each region. For those regions where no fires had occurred over the past 38 years, a fire return interval of 500 years was assumed.
Kasischke et al. (1994b) estimated that for forest type I, 35 % of the aboveground biomass and 37% of the ground-layer biomass are consumed during fire. For forest type 11, 15% of the aboveground biomass and 70% of the ground-layer biomass were consumed during fire. These estimates were derived for forests which were ~ 100 to ~ 150 years old. It is likely that the burn efficiency coefficient, b , is dependent on stand age For this study, however, it is assumed that b is constant.
For this study, it has been assumed that cf = 0.45.
Historical records and observations clearly show that fires in Alaska
are not limited to forested regions. Like forested regions, peatland and
tundra-covered areas contain thick mats consisting of dead, undecomposed
organic matter. When dry, this ground-layer material will burn quite readily.
While the occurrence of fires in tundra and peatlands in boreal regions
has been documented (Wein, 1976), virtually no information exists on the
amounts of biomass consumed during these fires. Kasischke e' al. (1994b)
showed that on average, 6 kg m-2 of biomass were consumed in
the ground layer during a fire in a black spruce forest in Alaska. For
this study, it is assumed that on average, 4 kg m-2 of biomass
are consumed in the ground layers of the peatlands and tundra areas in
Alaska based on the fact that the soils of areas containing these cover
types have higher moisture levels and are less susceptible to burning.
Biomass burning in boreal forests is likely to increase in response
to future global warming. To estimate the amounts of greenhouse gases released
during this fires will require accurate estimates of the locations and
extent of this burns, as well as regional models of biomass burning for
the forests found in the various regions.
Cahoon, D.R., Jr., B.J. Stocks, J.S. Levine, W.R. Cofer III, and J.M. Pierson, Satellite analysis of the severe 1987 forest fires in northern China and southeastern Siberia, J. Geo. Res. 1994.
French, N.H.F., E.S. Kasischke, L.L. Bourgeau-Chavez, and D. Barry, Mapping the location of wildfires in Alaska using AVHRR data, Int. J. Wildlands Fire (in press), 1994.
Gabriel, H.W. and G.F. Tande, A Regional Approach to Fire History in Alaska, BLM-Alaska Technical Report 9, Anchorage, Alaska, 34 pp., 1983.
Houghton, R.A., Biomass burning from the perspective of the global carbon cycle, in Global Biomass Burning: Atmospheric, Climatic and Biospheric Implications, edited by J.L. Levine pp. 321-325, The MIT Press, Cambridge, MA USA, 1991.
Kasischke, E.S., and French, N.H.F., Locating and estimating the areal extent of wildfires in Alaskan boreal forests using multiple season AVHRR NDVI composite data, Remote Sens. Environ. (in press), 1994.
Kasischke, E.S., French, N.H.F., Harrell, P., Christensen, N.L., Ustin, S.L., and Barry, D., 1993, Monitoring of wildfires in boreal forests using large area AVHRR NDVI composite data, Remote Sens. Environ., 44, 61-71, 1993.
Kasischke, E.S., N.L. Christensen, Jr., and B.J. Stocks, Fire, global warming and the mass balance of carbon in boreal forests, Ecol. Appl. (in review), 1994a.
Kasischke, L.L. Bourgeau-Chavez, and N.H.F. French, Biomass consumption during wildfires in black and white spruce forests in interior Alaska, Can. J. Forest Res. (in review), 1994b.
Kuchler, A.W., Potential vegetation map of the slate of Alaska, in National Atlas of the United States of America, edited by A.C. Gerlach, pp. 92, U.S. Geol. Survey, Washington, D.C., 1970.
Seiler, W. and P.J. Crutzen, Estimates of gross and net fluxes of carbon between the biosphere and atmosphere, Clim. Change, 2, 207-247, 1980.
Van Cleve, K, Oliver, L., Schlentner, R., Viereck, L.A., and Dyrness, C.T. 1983. Productivity and nutrient cycling in taiga l forest ecosystems, Can. J. For. Res., 13, 747-766, 1983.
Viereck, L.A., The effects of fire in black spruce ecosystems of Alaska and northern Canada, in The Role of Fire in Northern Circumpolar Ecosystems, ed. by R.W. Wein and D.A. MacLean, pp. 201 -220, John Wiley & Sons, Chichester, 1983.
Wahrhaftig, C., Physiological Divisions of Alaska. USDI Geol. Surv. Prof. Paper 482, 1965.
Wein. R.W., Frequency and characteristics of arctic tundra fires, Arctic, 29, 213-222, 1976.
Yarie, J., Forest fire cycles and life tables: a case study from interior Alaska, Can. J. For. Res., 11, 554-562, 1981.
Yarie, J., Forest Community Classification of the Porcupine River Drainage, Interior Alaska. and Its Application to Forest Management, U.S. Forest Service Tech. Report PNW-154, Portland, Oregon, U.S. Depart. of Agriculture, 63 pp., 1983.