Syntaxonomy of zonal dark-coniferous forests of southern taiga of the West Siberian plain and of humid low-mountains of the Altai-Sayan mounain region

2015 ◽  
pp. 85-107 ◽  
Author(s):  
N. N. Lashchinsky ◽  
A. Yu. Korolyuk

The dark-coniferous forests of the West Siberian southern taiga subzone are quite unique. They deter­mine a specific of the Ob’-Irtysh geobotanical field in a sense of V. B. Sochava (1948) together with the West Siberian zonation type (Shumilova, 1979). The main features of zonal southern taiga forests are: dominance of Abies sibirica in a tree layer; species-rich shrub layer; poor ground moss cover; well developed herb layer with a constant presence of nemoral species. We consider the southern taiga forests as hemi­boreal after L. Hдmet-Ahti (1963, 1981). We described the zonal dark-coniferous forests of southern taiga in Milio effusi–Abietetea sibiricae class first proposed by T. I. Zhitlukhina (1988) for the forests in the North-East Altai. Significant increasing of the area studied and existing syntaxa diversity make it necessary to change a diagnostic species group. A new combination of diagnostic species includes Abies sibirica, Padus avium, Lonicera xylosteum, Daphne mezereum, Rubus idaeus, Aconitum septentrionale, Dryopteris dilatata (incl. D. expansa), D. carthusiana, Urtica dioica, Milium effusum, Calamagrostis obtusata, Paris quadrifolia, Allium microdictyon, Stellaria bungeana, Oxalis acetosella, Circaea alpina. Most of Milio effusi–Abietetea sibiricae class communities occur in the West Siberian plain, which is relatively geologicaly young. Due to this fact a flora of southern taiga is mostly allochtonic formed by species migrations fr om the Eastern Europe and the Southern Siberian mountains. Among the diagnostic species the main dominants of tree layer (Abies sibirica) and herb layers (Calamagrostis obtusata and Aconitum septentrionale) have the North Asian distribution. Two shrub species Lonicera xylosteum and Daphne mezereum are European ones and two herbaceous species (Allium microdictyon and Stellaria bungeana) are represented in Europe by vicariant species. All other diagnostic species are Eurasian or Holarctic. Wide distribution of few species, in particular ferns, could be explained by the antiquity of taiga flora (Tolmachev, 1954). Typical habitats of Milio effusi–Abietetea sibiricae forests are the most humid areas with annual precipitation about 500–600 mm on plains and more than 800 mm in mountains. Soils on plains developed under these communities are deeply podzolised type with second humus horizon. In the low-mountains the deeply podzolised soddy-podzolic soils correlate to the area of Milio effusi–Abietetea sibiricae forests distribution. The northern lim it of southern taiga perfectly coincides with the southern border of the largest Pleistocene glaciations. The low mountains of Altai-Sayan system were never glaciated. The thick loess deposits help to survive some nemoral plant species in the isolated refuges. Milio effusi–Abietetea sibiricae class consists of two orders. The order Carici macrourae–Abietetalia sibiri­cae comprises zonal dark-coniferous forests of the West Siberian southern taiga subzone and their successional variants. Diagnostic species are the same as for Carici macrourae–Abietion sibiricae alliance and Aegopodio podagrariae–Abietetum sibiricae association: Gymnocarpium dryopteris, Rubus saxa­tilis, Carex macroura, Aegopodium podagraria, Viola selkirkii, Galium triflorum, Atragene sibirica, Actaea erythrocarpa, Ribes spicata, Stellaria holostea. It contains the alliance Carici macrourae–Abietion sibiricae and three associations. One of these was previously described by N. B. Ermakov but two others are new. Aegopodio podagrariae–Abietetum sibiricae association includes the primary zonal coniferous forests of the West Siberian southern taiga as well as successional stages after some catastrophic events (crown fires, windfall, etc.). Usually it is characterized by closed canopy with Abies sibirica dominance, species-rich shrub layer and well-developed herb layer with high coverage of Carex macroura, Aegopodium podagraria, Stellaria bungeana, Oxalis acetosella and Calamagrostis obtusata. Linnaeo borealis–Abietetum sibiricae association comprises the zonal coniferous forests grown in the northern part of southern taiga subzone. Its diagnostic species: Linnaea borealis, Trientalis europaea, Luzula pilosa, Orthilia secunda, Lycopodium annotinum, Vaccinium vitis-idaea are common for the Vaccinio-Piceetea class communities. In contrast with previous association Linnaeo borealis–Abietetum sibiricae communities are characterized by multi-dominant tree layer with slight predominance of Abies sibirica; shrub layer is sparse and not so species-rich, in herb layer the main dominants are Carex macroura, Oxalis acetosella, Calamagrostis obtusata, Gymnocarpium dryopteris and sometimes big ferns. Moss cover is about 20 to 40% of soil surface. The order Abietetalia sibiricae consists of low-mountain chernevaya taiga and dark-coniferous mountain forests of the Altai-Sayan humid sectors. A set of diagnostic species includes Ribes atropurpureum, Saussurea latifolia, Geranium albi­flo­­rom (incl. G. krylovii), Euphorbia lutescens, Myoso­tis krylovii, Viola uniflora, Dryopteris filix-mas, Heracleum dissectum, Trollius asiaticus, Anemonoides altaica, Corydalis bracteata, Erythronium sibiricum. The most of diagnostic species are north-Asian or south-Siberian ones. Many of them are mountainous restricted to the Altai-Sayan mountain system. This order includes one alliance Milio effusi–Abietion sibiricae previously described by T. I. Zhitlukhina and N. B. Ermakov. Seven associations belonging to this alliance were described and characterized by N. B. Ermakov (2003). When thinking about further development of the class syntaxonomy we expect the diversity increasing by serial communities of mixed and small-leaved forests and swampy forests on a plain. We do not discuss western and eastern class limits now. No doubt that distribution area of the new class is wider than the West Siberia but to describe its limits and an interaction with neighboring classes some additional materials are needed.

2021 ◽  
Vol 237 ◽  
pp. 01003
Author(s):  
Shijing He ◽  
Tingting Dou

Park green space is an important part of garden green space, concentrated expression of the diversity of urban plants. In order to explore the diversity of plants in the park, a typical site in Zhongshan Park in Wuhan was selected for this survey. The species importance, richness index, diversity index and evenness index were used to analyze the characteristics of plant diversity.There are a total of 184 plants of 114 genera and 64 families in Wuhan Zhongshan Park. Among them, there are 86 species of plants of 40 families and 64 genera, 60 species of plants of 26 families and 38 genera, and 26 species of herbs, 11 families and 15 genera.The richness was herb layer > tree layer > shrub layer.Pielou uniformity was herb layer > tree layer > shrub layer;Shannon-wiener diversity was herb layer > tree layer > shrub layer.Simpson diversity was herb layer > tree layer > shrub layer.The diversity of herbaceous plants in the park is high, and the index of shrub layer is generally low, with few species. Plants in the park grow well, some plants are not evenly distributed.


2017 ◽  
pp. 33-58
Author(s):  
O. V. Morozova ◽  
Yu. A. Semenishchenkov ◽  
E. V. Tikhonova ◽  
N. G. Belyaeva ◽  
M. V. Kozhevnikova ◽  
...  

The objectives of this paper are the reviewing nemoral herb spruce forests of European Russia (ER), elaborating diagnostic species combination, revealing species diversity, discussing syntaxonomical position, and validation of nemoral herb spruce forest syntaxa. The study concern 62 coenofloras (published and unpublished data from 11 regions of ER) and 448 rele­vés. The initial diagnosis of the association (Korotkov, Morozova, 1986; Zaugolnova, Morozova, 2004), origi­nally based on local and incomplete materials, was refined, as a result of the generalization of a vast literature and factual data. All nemoral herb spruce forests of ER belong to ass. Rhodobryo rosei–Piceetum abietis Korotkov 1986 (RP) with three subassociations: RP typicum, RP abietetosum sibiricae and RP caricetosum pilosae. The issues of syntaxonomic assignment of the association to the higher units are discussed. The position of association within the class Carpino-Fagetea, order Carpinetalia and alliance Querco-Tilion was justified by predominance of nemoral species in lower layers of communities. Diagnostic species of association (Picea abies (upper layer), Athyrium filix-femina, Circaea alpina, Daphne mezereum, Dryopteris expansa, Gymnocarpium dryopteris, Mycelis muralis, Oxalis acetosella, Phegopteris connectilis, Pyrola rotundifolia, Stellaria nemorum; Cirriphyllum piliferum, Plagiochila porelloides, Plagiomnium affine, P. medium, Rhodobryum roseum, Sciuro-hypnum starkei, S. curtum) are identified by fidelity index (Chytrý et al., 2002) and largely coincide with species of suballiance Tilio-Piceenion (Morozova, 2016). Alliance of Eastern European oak and lime tree forests Querco-Tilion is divided into two suballiances including proper deciduous forests (Querco-Tilienion) and spruce forests with nemoral herb and moss layers (Tilio-Piceenion), reflecting the zonal features of deciduous-coniferous forests in ER. The specific traits of the association communities are the species polydominance and total predominance of nemoral species in the lower layers. Thus, nemoral species can be considered as a collective dominant, with a cover approximately equal to or exceeding that of Oxalis acetosella (Vasilevich, Bibikova, 2004). Dominant species in the herb-subshrub layer vary not only due to the local conditions, but also to the age of forest stands. O. acetosella, as well as Aegopodium podagraria, Carex pilosa, Galeobdolon luteum, Galium odoratum, Mercurialis perennis, Pulmonaria obscura, Stellaria holostea, and some fern species can predominate. For subassociation, an ecological characteristics estimated by Ellenberg indicator scales (Ellenberg et al., 1991) are given. The floristic originality of syntaxa and the role of environmental factors are demonstrated by the method of nonlinear multidimensional scaling (NMDS). Differentiation of the internal structure of the association at the lower hierarchy levels is difficult, since these forests are a very polymorphic group regarding the dominating species. The predominance of one or combination of several species is related to speci­fic environments and can be identified at the level of the variants, which is reflected in development of regional classifications (Semenishchenkov, Kuzmenko, 2011; Morozova, Tikhonova, 2012; Semenishchenkov, 2012). The area of eastern European nemoral herb spruce forests covers the territory from the east of the Baltic countries to the Volga river. Communities of association represent a zonal type of vegetation in the broad-leaved coniferous subzone and southern half of the southern taiga, but are extrazonal both in the north and south of their distribution. These forests occur on moraine loamy plains: in the southern taiga — mainly on the tops and slopes of hills, while in the broad-leaved coniferous subzone — on well drained plains and ­gentle slopes. Subassociations are differentiated by their geographical location: RP typicum represents west and central nemoral herb spruce forests, RP abietetosum occurs in the north-east of association range and RP caricetosum — in the south. For the most distinctive subassociation RP abietetosum character are the presence of Abies sibirica, hydrophylous and some species of Siberian tall herbs, and a smaller proportion of nemoral species. The number of species in the coenofloras is not ­being changed on the latitudinal gradient, but the species richness of the communities, as well as the cover of the lower layers, decrease southwards. Perhaps this is due to the increased presence of hazel, which creates a pronounced level of the undergrowth in the RP caricetosum. The floristic comparison and proposed concept of the nemoral herb spruce forests syntaxonomy make the regional syntaxonomic units comparable in volume and allow to adequately outline the modern range of forests of this type in ER.


2012 ◽  
Vol 518-523 ◽  
pp. 5302-5305
Author(s):  
Ren Yan Duan ◽  
Min Yi Huang ◽  
Zhi Gao Wang ◽  
Zhong Xin Zhang

Flora composition and species diversity features of Pseudolarix amabilis community at the Yaoluoping natural reserve in Anhui Province were analyzed. According to the statistics from 4 sample plots, there are 88 species (including varieties) of 77 genus belonging to 48 families of vascular plants. There are various plants in the community of Pseudolarix amabilis, and its family and genus are of scattered composition. Their floral composition is complicated. In terms of geographical composition of seed plant genus, most of them are distributed in the temperate zone. The species diversity of shrub layer is the highest, the tree layer is the second, and the herb layer is the lowest in the vertical structure of the community. The species diversity index of different layers shows: shrub layer>tree layer>herb layer.


2013 ◽  
Vol 726-731 ◽  
pp. 4172-4176
Author(s):  
Sheng Li ◽  
Hua Dong Ren ◽  
Liang Xue ◽  
Xiao Hua Yao

The space instead of time method was used to determine the species diversity and soil property in different succession stages in Karst rocky desertification area, in China. The species diversity of herb layer was digressive and that of tree layer, shrub layer and the whole community were increased first and then decreased, the peak value appeared in the rattan thorn scrub stage, the lowest appeared in the grass stages. At the beginning of succession, the species diversity of herb layer was higher than that of shrub layer. With the closing time increased, the diversity of the shrub layer increased more than that of herb layer. There had the same change trend in velocity nitrogen, organic matter, total nitrogen and total phosphorus. There was significantly linear positive correlation between the total nitrogen, phosphorus, magnesium, calcium, pH, available phosphorus and the species diversity and richness of the herb layer.


2003 ◽  
pp. 28-40 ◽  
Author(s):  
L. L. Zanokha

The 2 new associations, Carici stantis—Salicetum reptantis and Salico-Polemonietum acutiflori, are described within the all. Caricionstantis of the class Scheuchzerio-Caricetea fuscae R. Tx. 1937 for the northern belt of the typical tundra subzone of Taymyr. The diagnostic species group of the first syntaxon includes plants typical of sites with excessive watering. The ass. Carici stantis—Salicetum reptantis is restricted to bottoms or lower parts of the watershed and moun­tain terrace slopes. The ecological regime of these sites is subject to slight variations reflected in presence/ absence of certain species. Due to floristic differences, the association is subdivided into several subassociations which form a topographic-ecological series along the humidity gradient: epilobietosum palustris→ptilidietosum ciliaris→typicum→petasitetosum frigidi. The ass. Carici stantis—Salicetum reptantis is referred to the all. Caricionstantis which also includes the associations Meesiotriquetris—Caricetumstantis and Pooarcticae—Dupontietumfisheri (also described from the Ragozinka R. basin); the latter occur in the wet depres­sions between sloping hills and the flowing valleys, respectively. If compared to these two, the ass. Carici stantis—Salicetum reptantis is shown to hold an intermediate position between them. The ass. Salico-Polemonietum acutiflori with the 2 variants, Salix lanata and S. reptans, represents various variants of mire vegetation which have under­gone zoogenic transformation (by lemmings). The stands size 1—1.5 m2 in space. The diagnostic species group comprises plants common of the wet mossy stream banks. The association is referred to the all. Caricion stantis, although many diagnostic species of the alliance are not present in its composition. When the new data are available, the association is probable to be separated into an independent alliance.


2021 ◽  
Vol 76 (1) ◽  
pp. 1-10
Author(s):  
L. G. Bogatyrev ◽  
A. I. Benediktova ◽  
M. M. Karpukhin ◽  
V. M. Telesnina ◽  
N. I. Zhilin ◽  
...  

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