|
|
![]() |
Each forest type had its own elevation distribution but all have overlapping
slope ranges. A tendency for forests to be distributed on north facing
aspects at their lowest elevational limits and on west or south facing
aspects at their highest elevation was observed. This study will discuss
an ecological modeling application that interfaces statistical models and
GIS output using GRID. The resulting ecological rules describe physiographic
characteristics for each forest type and the procedures used for developing
these rules may themselves provide a useful research tool for predicting
new vegetation distributions under different climate scenarios. The new
GIS developed maps will provide a direct view of the topographic dependence
of different ecological communities and vegetation cover in a complex heterogeneous
environment. This approach to integrated environmental analysis will provide
better information for planning and management of environmental resources.
Much research has been done by California ecologists to define the relationships between forests and environmental variables. Because of the Mediterranean climate in California, precipitation (both timing and abundance) is one of the critical physical factors controlling the distribution of vegetation (Barbour, 1988; Rundel et al., 1988; Major, 1989). Soil moisture gradients are dependent on the site conditions that are themselves largely a function of aspect, slope, soil type, and profile (Hole and Campbell, 1985; Ward and Robinson, 1990). Although past reviews (e.g., Rundel et al., 1988) have summarized the physical, physiological and ecological relationships for these forests, they have not been examined in the synoptic view possible with GIS techniques.
This paper will identify and illustrate some spatial relationships between
the distribution and abundance of Sierran forests and topographic features.
This preliminary work is an initial step in a longer-term research effort
to model dynamic ecosystem processes for predicting future ecological characteristics
in the Sierra Nevada.
Most data in this study were obtained from the U.S. Forest Service, including digitalisheries in the region. The model represents a new synthesis of GIS, remote sensing, and modeling on a critically important hydrologic problem.
Mr. Xiao has nine years of remote sensing research at the Chinese Academy of Sciences, Remote Sensing Application Center of Ministry of Water Resources P.R.C. (China), before coming to U.C. Davis as a graduate student in 1992. He has completed his MS degree in two years (GPA is 4.0 at UCD), during which time he has become proficient in using the ARC/Info GISing these data.
Slope was classified into four groups, low (0-30%), medium (31-50%),
high (5170%), and very steep (>70%). Aspects were divided into 8 equal
groups between 0 and 360 degrees (Table 2).
Elevation contours at 100 meter intervals were used in the analysis. Furthermore,
basic descriptive statistics were spatially plotted and other map overlays
were used in the study.
Eighteen conifer and broadleaf tree species grow within the ENF, and occur in a wide range of tree size classes and densities. However, only six species are dominant (Table 3) and these comprise 89.3% of all forested land in the EMF. The most abundant forest classes are mixed conifer pine, mixed conifer fir, ponderosa pine, red fir, sub-alpine conifer and non-forest, respectively (Table 3). Most of these forests (over 77% of the total vegetation cover) are composed of trees in the small and medium size classes and these units have a mean density class rating of more than 40% crown closure.
About 70% of all forests today occur with slope gradient less than 30%, and over 20% occurs in the next slope class, between 31 to 50% (Table 1). Eighty-six percent of forests are distributed between elevations of 1000 to 2600 meters. Table 3 shows that forests are distributed over the full elevation range with some, e.g., ponderosa pine, distributed primarily at the lower elevations and sub-alpine forest at highest elevations, and the rest in intermediate elevation zones. However, when the analysis is restricted to forests containing the largest trees (class 3G and 4N), they are found to be distributed primarily in the higher elevations. The distributions of younger tree classes were disproportionately abundant at lower elevations in the forest. The small and medium timber size classes are found throughout the range of density classes and stand density was not significantly related to elevation. The forest types, size classes, and the densities, were not significantly associated with aspect in the forest except that the eastern aspects had the lowest vegetation cover. We found that 78% of the total forest cover was within the size 3 and 4 timber classes (small and medium timber) shown in Table 4, and that 54% of the forest cover had medium and high (greater than 40%) crown closure. Most timber areas of small and medium size classes with dense crown closures were within the slope ranges between 0 and 50%. These findings are consistent with an ENF composed of predominantly younger forests or those in an early to mid-successional status relative to forests of predominantly late seral characteristics (lower density forests of high crown closure composed of largest size-class trees). Historic records indicate that the Sierra Nevada forests have always supported a mosaic of variable aged forests. Evaluation of the age distribution structures in relation to the historic distributions was not attempted in this study.
Figure 2 shows that the major forests differ from each other with respect to abundance, aspect, elevation, and slope. The patterns of forest distributions are somewhat asymmetric with aspect. These patterns could be related to climate and energy balance constraints or a both climate and land use.
On the basis of these findings, we believe that further research focused on modeling the ecological relationships between topographic features and vegetation distribution in the ENF will be useful. The vegetation distribution integrates the complexity of the physiographic factors, therefore, it is essential to characterize the environmental variables directly associated with distribution. Using a multivariate statistical approach, an integrated environmental index can be identified to quantify this response. This type of processes-based index is derived from intermediate variables obtained from a spatial analysis of climate data in the GIS, which is used to drive a model of physiological functioning (e.g., Running and Coughlan, 1988; Running and Grower, 1991, Running and Hunt, 1993; Bonan, 1989). A statistical model can be built using methods employed in the "Chipmunk" model (Ed Royce, UC Davis, personal communication). Such a model can be constructed to predict the vegetation cover for each forest species based on topographic and climate constraints. This simulation method can be useful for predicting the vegetation dynamics under different scenarios. In addition, various additional kinds of spatial relationships can be identified through the simulation modeling effort.
To conclude, we found that the distribution of forest age and size classes in the ENF was strongly related to the topographic features of elevation, slope, and aspect. Some current patterns appear to be related to the pattern of forest extraction in the past century and others to climate conditions. The analysis also provided us with a clear direction for developing a model to describe the spatial relationships among the factors. GIS is the critical tool to a landscape scale ecological analysis.
Acknowledgments: We wish to thank Ralph Warbington, USFS (Sacramento,
CA) and the Sierra Nevada Ecosystem Project (SNEP) for providing us with
the U.S. Forest Service Forest Timber Inventory data base for the Eldorado
National Forest and Steve Beckwitt, Sierra Biodiversity Institute for assisting
us with the AML elevation classification.
Bonan, G.B. and Shugart, H.H. 1989. Environmental factors and ecological processes in boreal forests. Ann. Rev. Ecol. Systm. 20: 1-28.
Rundel, P.W., Parsons, D.J., and Gordon, D.T., 1988. Montane and subalpine vegetation of the Sierra Nevada and Cascade Ranges. in Barbour, M.G. and Major, J. eds: Barbour, M.G. and J. Major, eds: Terrestrial vegetation of California, California Native Plant Society. p. 559601.
Clements, E.S. 1920. Plant indicators: the relation of plant communities to process and practice. Carnegie Institution of Washington. p. 290.
ESRI, 1992. ARC/TNFO GRID Users Guide. Environmental Systems Research Institute, Redlands, CA.
Hole, F.D., and Campbell, J.B. 1985. Soil Landscape Analysis. Rowman and Allanheld Publ., Towata, NJ, p. 191.
Major, J. 1988. California Climate in relation to vegetation, in Barbour, M.G. and J. Major, eds: Terrestrial vegetation of California, California Native Plant Society. p. 11-74.
Major, J. 1982. Climate, in Burke, M.T., Curry, R., Major, J. and D.W. Taylor, eds: Natural landmarks of the Sierra Nevada, Department of Botany, University of California, Davis. p. 1228.
Royce, E.B. 1993. Climate effects on the distribution of vegetation in the upper montane zone of the southern and central Sierra Nevada range -- the Chipmunk climate model. (Unpublished materials) Department of Environmental Horticulture, University of California, Davis.
Running, S.W. and Coughlan, J.C. . 1988. FOREST-BGC, a general model of forest ecosystem processes for regional applications. I. Hydrologic balance, canopy gas exchange and primary production processes. Ecol. Model. 42: 125-154..
Running, S.W. and Grower, S.T. 1991. FOREST-BGC, a general model of forest ecosystem processes for regional applications. II. Dynamic carbon allocation and nitrogen budgets. Tree Physiol. 9: 147-160.
Running, S.W. and Hunt, E.R., Jr. 1993. Generalization of a forest ecosystem process model for other biomes, BIOME-BGC, and an application for global scale models. In Scaling Physiological Processes: Leaf to Globe (J. Elhringer and C. Fields, eds.) Academic Press, p. 141-158.
Ustin, S., Szeto, L.H.., Xiao, Q.F., Hart, Q.J., and E.S. Kasischke. 1994. Vegetation mapping of forested ecosystem in interior central Alaska. IGARSS 94: Proceedings of the International Geosciences and Remote Sensing Symposium, T. I. Stein, ed., Pasadena, CA August 8-12, 1994.
Ward, R.C., and Robinson, M. 1990. Principles of Hydrology. McGraw-Hill Book Co. San Francisco, CA, p. 365.