Model reconstruction of restored taiga forest cover

2013 ◽  
Vol 3 (6) ◽  
pp. 493-504 ◽  
Author(s):  
O. V. Smirnova ◽  
D. V. Lugovaya ◽  
T. S. Prokazina
2018 ◽  
Vol 14 (1) ◽  
pp. 51-60
Author(s):  
Emilian DANILA ◽  
VALENTIN Hahuie ◽  
Puiu Lucian GEORGESCU ◽  
Luminița MORARU

2019 ◽  
pp. 68-72
Author(s):  
E. A. Volkova

A monograph “Vegetation and biotopes of the “Narochansky” National Park was published in Minsk, Belarus in 2017, edited by A. V. Pugachevsky (Grummo et al., 2017). It includes the Map of terrestrial vegetation (S. 1 : 60 000) and the Map of biotopes (S. 1 : 60 000). Some small-scale maps such as the Map of changes in forest cover of the “Narochansky” National Park for the period 1985–2016, the Map of forest loss in the “Narochansky” National Park for the period 1985–2016 and a series of inventory and analytical maps on the basin of the Naroch Lake are given. This monograph can be considered as a small regional Atlas with detailed explanatory texts to the maps. It presents the experience on vegetation mapping accumulated in the Laboratory of Geobotany and Vegetation mapping of the Institute of Experimental Botany of the National Academy of Sciences of Belarus. Despite some critical comments, mainly concerning the biotope map, this publication of Belarusian geobotanists deserves an approval. They received the full answers to the questions posed: “What do we protect?” and “What is a current state of the vegetation of the National Park and the main trends of its dynamics? Cartographic design is made at a high level; the maps have both scientific and practical importance in the planning of environmental and economic activities.


1996 ◽  
pp. 51-54 ◽  
Author(s):  
N. V. M. Unni

The recognition of versatile importance of vegetation for the human life resulted in the emergence of vegetation science and many its applications in the modern world. Hence a vegetation map should be versatile enough to provide the basis for these applications. Thus, a vegetation map should contain not only information on vegetation types and their derivatives but also the geospheric and climatic background. While the geospheric information could be obtained, mapped and generalized directly using satellite remote sensing, a computerized Geographic Information System can integrate it with meaningful vegetation information classes for large areas. Such aft approach was developed with respect to mapping forest vegetation in India at. 1 : 100 000 (1983) and is in progress now (forest cover mapping at 1 : 250 000). Several review works reporting the experimental and operational use of satellite remote sensing data in India were published in the last years (Unni, 1991, 1992, 1994).


2018 ◽  
pp. 107-130 ◽  
Author(s):  
T. V. Chernenkova ◽  
O. V. Morozova ◽  
N. G. Belyaeva ◽  
M. Yu. Puzachenko

This study aimed at an investigation of the structure, ecology and mapping of mixed communities with the participation of spruce, pine and broad-leave trees in one of the regions of broad-leave–coniferous zone. Despite the long history of the nature use of the study area, including forestry practices (Kurnayev, 1968; Rysin, Saveliyeva, 2007; Arkhipova, 2014; Belyaeva, Popov, 2016), the communities kept the main features of the indigenous forests of the broad-leave–coniferous zone ­— the tree species polydominance of the stands, the multilayer structure of communities and the high species diversity. In the course of field works in the southwestern part of the Moscow Region (2000–2016) 120 relevés were made. Spatial structure, species composition as well as cover values (%) of all vascular plants and bryophytes were recorded in each stand. The relevés were analysed following the ecology-phytocenotic classification approach and methods of multivariate statistical analysis that allowed correctly to differentiate communities according the broad-leave species participation. The accuracy of the classification based on the results of discriminant analysis was 95.8 %. Evaluation of the similarity of the selected units was carried out with the help of cluster analysis (Fig. 12). Clustering into groups is performed according to the activity index of species (A) (Malyshev, 1973) within the allocated syntaxon using Euclidean distance and Ward’s method. The classification results are corrected by DCA ordination in PC-ORD 5.0 (McCune, Mefford, 2006) (Fig. 1). Spatial mapping of forest cover was carried out on the basis of ground data, Landsat satellite images (Landsat 5 TM, 7 ETM +, 8 OLI_TIRS), digital elevation (DEM) and statistical methods (Puzachenko et al., 2014; Chernenkova et al., 2015) (Fig. 13 а, б). The obtained data and the developed classification refine the existing understanding of the phytocenotic structure of the forest cover of the broad-leave–coniferous zone. Three forest formation groups with different shares of broad-leave species in the canopy with seven groups of associations were described: a) coniferous forests with broad-leave species (small- and broad-herb spruce forests with oak and lime (1)); broad-herb spruce forests with oak and lime (2); small- and broad-herb pine forests with spruce, lime, oak and hazel (3); broad-herb pine forests with lime, oak and hazel (4)), b) broad-leave–coniferous forests (broad-herb spruce–broad-leave forests (5)), and c) broad-leave forests (broad-herb oak forests (6), broad-herb lime forests (7)). In the row of discussed syntaxa from 1 to 7 group, the change in the ratio of coniferous and broad-leave species of the tree layer (A) reflects re­gular decrease in the participation of spruce in the plant cover (from 66 to 6 %; Fig. 3 A1, A2) and an increase in oak and lime more than threefold (from 15 to 65 %; Fig. 4 a). Nemoral species predominate in the composition of ground layers, the cove­rage of which increases (from 40 to 80 %) in the range from 1 to 7 group, the coverage of the boreal group varies from 55 to 8 % (Fig. 11) while maintaining the presence of these species, even in nemoral lime and oak forests. In forests with equal share of broad-leave and coniferous trees (group 5) the nemoral species predominate in herb layer. In oak forests (group 6) the species of the nitro group are maximally represented, which is natural for oak forests occurring on rich soils, and also having abundant undergrowth of hazel. Practically in all studied groups the presence of both coniferous (in particular, spruce) and broad-leave trees in undergrowth (B) and ground layer (C) were present in equal proportions (Fig. 3). This does not confirm the unambiguity of the enrichment with nemoral species and increase in their cover in complex spruce and pine forests in connection with the climate warming in this region, but rather indicates on natural change of the main tree species in the cenopopulations. Further development of the stand and the formation of coni­ferous or broad-leave communities is conditioned by landscape. It is proved that the distribution of different types of communities is statistically significant due to the relief. According to the results of the analysis of remote information, the distribution areas of coniferous forests with broad-leave species, mixed and broad-leave forest areas for the study region are represented equally. The largest massifs of broad-leave–coniferous forests are located in the central and western parts of the study area, while in the eastern one the broad-leave forests predominate, that is a confirmation of the zonal ecotone (along the Pakhra River: Petrov, Kuzenkova, 1968) from broad-leave–coniferous forests to broad-leave forests.


Author(s):  
V. N. Suleimanova ◽  
N. Yu. Egorova

The object of our research was one of the most common orchids in the world – Cypripedium calceolus L. As a rare species, it is listed in the Red book of the Russian Federation (3 category of rarity) [8], the Kirov region (3 category of rarity) [9], as well as in the Red books of 59 regions of the Russian Federation [2]. Limiting factors in the Kirov region are the violation of habitats as a result of anthropogenic impacts – deforestation, recreation, collection for bouquets, digging, reducing the number of species. Studies on the study of C. calceolus in the Kirov region are isolated [10–12]. The purpose of this work is to identify phytocenotic parameters and environmental conditions of C. calceolus habitats within the southern taiga fragment of the range. Studies of ecological and cenotic conditions of C. calceolus habitats were conducted in southern taiga forest ecosystems within the Kirov region (Slobodskaya, Afanasyevsky districts) (See table 1) in the period from 2012 to 2019. The studied habitats of C. calceolus are confined to non-morally-boreal-small-grass and grass spruce forests (Melico nutantis-Piceetum abietis subass. typicum, Maianthemo-Piceetum subass. typicum var. typical) (See fig. 1), pine trees with fir and spruce of various grasses (Melico nutantis-Pinetum sylvestris var. Lathyrus vernus). The growth of C. calceolus on the technogenically disturbed substrate of an old spent limestone quarry overgrown with coniferous rocks and various grasses was also noted. All the studied biotopes are characterized by a large constancy of non-moral species with not significant coverage of mosses. The stand of spruce forest types is dominated by Picea abies, pine-Pinus sylvestris. Abies sibirica occurs as an impurity. The undergrowth layer has a diverse species composition: Sorbus aucuparia, Frangula alnus, Lonicera xylosteum, Yuniperus communis, Daphne mezereum. In this tier of most studied phytocenoses there is a Atragene sibirica. The grass-shrub layer is also very diverse, which determines the high specificity of these communities. In addition to species of boreal small grass (Maianthemum bifolium, Orthilia secunda, Luzula pilosa, Rubus saxatilis), the presence of non – morals is characteristic-Lathyrus vernus, Melica nutans, Stellaria holostea, Asarum europaeum. Moss-lichen layer is fragmentary (covering up to 45 %), Pleurozium schreberi and Hylocomium splendens act as sodominants. Phyto-indication of the studied C. calceolus habitats according to ten ecological scales of D. N. Tsyganov (See table 2, Fig. 2) showed that in relation to the complex of all environmental factors, the studied species is mesovalent (MV) (It total = 0.54) and has an average level of lability in relation to the studied environmental factors. In relation to the complex of all environmental factors, C. calceolus is a mesobiont species. On a scale of soil acidity, the species is semistarvation at termokhimicheskie and apolitically scale and dial illumination-shading – metavalent on the scale of the wealth of the soil nitrogen – hemimillennial at createmotions scale and the scale of continentality of the climate avivamento. Only on the scale of soil moisture and the scale of soil salt regime, C. calceolus is stenovalent, which indicates a very limited range of possible habitats for this factor. The species, in the studied habitats, realizes from 4.61 to 23.84 % of its potential according to the studied factors. For C. calceolus, the results obtained allow us to extend the scale of soil acidity by 0.75 degrees to the right. According to the other scales, the values of the ecological space of the studied CP are placed in the ranges given by D. N. Tsyganov for this type Edaphic conditions of C. calceolus on the scale of soil moisture correspond to regimes from dry-saline to wet-forest-saline; on the factor of soil salt regime-poor soils; soil acidity – acidic-slightly acidic soils; soil richness in nitrogen – nitrogen – poor soils; moisture variability-soils with relatively stable and poorly variable moisture.


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