One of the most difficult tasks in large-scale vegetation mapping is the clarification of mechanisms of the internal integration of vegetation cover territorial units. Traditional way of searching such mechanisms is the study of ecological factors controlling the space heterogeneity of vegetation cover. In essence, this is autecological analysis of vegetation. We propose another way of searching the mechanisms of territorial integration of vegetation. It is connected with intracoenotic interrelation, in particular, with the changing role of edificator synusium in a community along the altitudinal gradient. This way of searching is illustrated in the model-plot in subarctic tundra of Central Chukotka. Our further suggestion concerns the way of depicting these mechanisms on large-scale vegetation map.
As a model object we chose the catena, that is the landscape formation including all geomorphjc positions of a slope, joint by the process of moving the material down the slope. The process of peneplanation of a mountain system for a long geological time favours to the levelling the lower (accumulative) parts of slopes. The colonization of these parts of the slope by the vegetation variants, corresponding to the lowest part of catena is the result of peneplanation. Vegetation of this part of catena makes a certain biogeocoenotic work which is the levelling of the small infralandscape limits and of the boundaries in vegetation cover. This process we name as the continualization on catena. In this process the variants of vegetation in the lower part of catena are being broken into separate synusiums. This is the process of decumbation of layers described by V. B. Sochava.
Up to the slope the edificator power of the shrub synusiums sharply decreases. Moss and herb synusium have "to seek" the habitats similar to those under the shrub canopy. The competition between the synusium arises resulting in arrangement of a certain spatial assemblage of vegetation cover elements. In such assemblage the position of each element is determined by both biotic (interrelation with other coenotic elements) and abiotic (presence of appropriate habitats) factors. Taking into account the biogeocoenotic character of the process of continualization on catena we name such spatial assemblage an exolutionary-biogeocoenotic series.
The space within each evolutionary-biogeocoenotic series is divided by ecological barriers into some functional zones. In each of the such zones the struggle between synusiums has its individual expression and direction.
In the start zone of catena (extensive pediment) the interrelations of synusiums and layers control the mutual spatial arrangement of these elements at the largest extent. Here, as a rule, there predominate edificator synusiums of low and dwarfshrubs. In the first order limit zone (the bend of pediment to the above part of the slope) one-species herb and moss synusiums, oftenly substituting each other in similar habitats, get prevalence.
In the zone of active colonization of slope (denudation slope) the coenotic factor has the least role in the spatial distribution of the vegetation cover elements. In particular, phytocoenotic interactions take place only within separate microcoenoses of herbs, mosses and lichens. In the zone of the attenuation of continualization process (the upper most parts of slope, crests) phytocoenotic interactions are almost absent and the spatial distribution of vegetation cover elements depends exclusively on the abiotic factors. The principal scheme of the distribution of vegetation cover elements and the disposition of functional zones on catena are shown on block-diagram (fig. 1).
Quantitative estimates of average geomagnetic axial dipole dominance in deep geological time
