scholarly journals CULTIVATED SPECIES OF PLANTS IN THE COMPOSITION OF FLORA OF THE SOUTHERN TRANS-URAL REGION

Author(s):  
N.I. Naumenko

This work was carried out with the aim of inventorying and analyzing cultivated species as part of the adventive component of the flora of the Southern Trans-Urals within the boundaries of the Kurgan Region and adjacent areas of the adjacent regions of Russia and Kazakhstan. In the territory under consideration, 296 species and 8 hybrids from 201 genera and 68 families of vascular plants, more or less regularly grown in open ground, and registered outside of cultivation sites, are registered. The list of cultivated plant species was 18.8 % of the flora of the Southern Trans-Urals. The overwhelming majority of plants cultivated in the region belong to ergasiophytes (226 taxons, or 76.4 % of the list of cultivated plants), which are unstable without care and are rarely observed outside cultivation sites. The group of plants more or less successfully entrenched in natural and (or) anthropogenically transformed communities is represented by 78 taxa (26.4 % of the total number of cultivated species). By the nature of their use, the most extensive is the list of ornamental herbaceous plants (119 taxa, or 39.9 % of the total number of cultivated species), ornamental trees and shrubs (62 species). The composition of food, aromatic and medicinal cultures is also significant (98 species). The list is closed by feed (16 species) and industrial crops (3 species). Systematically, taxa and hybrids cultivated in the Trans-Urals are represented by 68 families, the most numerous are Asteraceae (40 taxa), Rosaceae (29) and Fabaceae (25). In the spectrum of life forms of plants cultivated in the Trans-Urals, grassy monocarpics are leading: annuals (119 species, 39.9 %) and biennials (11 species, 3.7 %). By the nature of the primary range, the plants cultivated in the Trans-Urals are divided into 16 groups. Taxa with “western” origin are the most numerous: American (73 species), European (55 species), Mediterranean-South European (49 species), Mediterranean-Asian (41 species).

2010 ◽  
Vol 10 (4) ◽  
pp. 205-213 ◽  
Author(s):  
Silvana Masciadri ◽  
Ernesto Brugnoli ◽  
Pablo Muniz

In Uruguay, as well as in other regions of the world, IAS cause negative impacts on natural and managed ecosystems. The use of databases is a helpful tool to elaborate different strategies for prevention and control, and to develop policies and scientific analyses related to IAS. The database of IAS in Uruguay (InBUy) was developed during two time periods (2006-2007 and 2009-2010). It currently contains information on 33 specialists of different taxonomic groups, 14 research projects, 185 references, 351 species and 4,715 records, with vascular plants having both the highest number of species and records. Among vascular plants, herbaceous life forms are the most strongly represented, followed by trees and shrubs. Within animals, the fishes and mollusks are the most important groups. Analysis of the native distribution areas of IAS showed that most are indigenous from Europe, followed by Asia and Oceania. Data showed that introductions of IAS into Uruguay are mainly intentional (67%), so efforts should be focused on policies and rules in order to control the entrance of exotic organisms and prevent new invasions. The geography of the compiled dataset shows the main impact is along the coastline, where the highest exotic species richness and records occurs, and also the most biological invasions. The InBUy database is up-to-date and has successfully contributed to the creation of an official IAS list for Uruguay and both a National and a Coastal Geographic Information System. It has also been used for developing consciousness about this important threat to biodiversity, at both national and regional scales.


2020 ◽  
Vol 169 ◽  
pp. 03005
Author(s):  
Alaa Dabbagh

Open mining of sand is executed in the sand pits. After completion of the work sand pits are usually recultivated: firstly they are graded and then planted with trees and shrubs, but very often sand pits are abandoned to regenerate themselves. The sand pit becomes a source of dust and a hardly healed wound on the earth’s body. In order to provide an adequate revegetation on such substrates, it is necessary to study biomorphological peculiarities of growing plants in a very specific environment characterized by high stiffness of slopes and high mobility of the substrate. The material for our study collected from Moscow Region sand pits in the Russian federation. Plants were collected from both northern and southern exposure slopes. Our work is based on the geobotanical descriptions made according to standard method on experimental sites of 5x5 m2. The results of the undertaken shows that Compositae, Gramineae, Fabaceae are the most representative of the surveyed one hundred twenty seven species of higher vascular plants from 29 families. Diversity on the southern slopes was more than on the northern ones. Species diversity is determined by the successions occurring spontaneously after a rough anthropogenic intervention, under the influence of such environmental factors as lighting, moisture, texture and richness of soil. The spectrum of life forms showed that the overwhelming majority according to K. Raunkiru are hemicryptophytes. Perennial herbaceous polycarpics are dominant in the spectrum of life forms, according to I.G. Serebryakov.


2020 ◽  
pp. 75-99
Author(s):  
O. I. Sumina

One of the thermokarst relief forms is baidzharakh massif — the group of mounds separated by trenches formed as a result of the underground ice-wedge polygonal networks melting (Fig. 1). Study of baidzharakh vegetation took place on the northeast coast of the Taimyr Peninsula (the Pronchishcheva Bay area) and on the New Siberian Islands (the Kotelny Island) in 1973–1974 (Sumina, 1975, 1976, 1977a, b, 1979 et al.). The aim of this paper is to produce the classification of baidzharakh mound and trenches communities according to the Brown-Blanquet approach (Westhoff, Maarel, 1978) and to compare these data with the community types earlier established on domination principle (Sumina, 1975 et al.). The information obtained in the 1970s could be helpful in a comparative assessment of the thermokarst process dynamics over the past 4 decades, as well as for comparing these processes in other regions of the Arctic. Both studied areas are located in the northern part of the arctic tundra subzone. On the Taimyr Peninsula (and in particular in the Pronchishcheva Bay area) the plakor (zonal) communities belong to the ass. Salici polaris–Hylocomietum alaskani Matveyeva 1998. Our relevés of plakor tundra on the Kotelny Island demonstrate similarity with the zonal communities of the northeast coast of the Taimyr Peninsula (Table 2). Relevés of communities of thermokarst mounds were made within their boundaries, the size of ~ 30 m². In trenches sample plots of the same area had rectangular shape according to trench width. Relevés of plakor tundra were made on 5x6 m plots. There were marked: location in relief, moistening, stand physiognomy, nanorelief, the percent of open ground patches and degree of their overgrowing, total plant cover, that of vascular plants, mosses, and lichens (especially — crustose ons), and cover estimates for each species. The shape of thermokarst mounds depends on the stage of thermodenudation processes. Flat polygons about 0.5 m height with vegetation similar to the plakor tundra are formed at the beginning of ice melting (Fig. 3, a), after which the deformation of the mounds (from eroded flat polygon (Fig. 3, b) to eroded conical mound (Fig. 3, c). Such mounds of maximal height up to 5 m are located on the middle part of steep slopes, where thermodenudation is very active. The last stage of mound destruction is slightly convex mound with a lumpy surface and vegetation, typical to snowbed sites at slope foots (Fig. 3, d, and 5). Both on watersheds and on gentle slopes mounds are not completely destroyed; and on such elongated smooth-conical mounds dense meadow-like vegetation is developed (Fig. 6). On the Kotelny Island thermokarst mounds of all described shapes occur, while in the Pronchishcheva Bay area only flat polygons, eroded flat polygons, and elongated smooth-conical mounds are presented. Under the influence of thermodenudation the plakor (zonal) vegetation is being transformed that allows to consider the most of mound and trench communities as the variants of zonal association. On the base of 63 relevés, made in 14 baidzharakh massifs, 2 variants with 7 subvariants of the ass. Salici polaris–Hylocomietum alaskani Matveyeva 1998 were established, as well as 1 variant of the azonal ass. Poo arcticae– Dupontietum fisheri Matveyeva 1994, which combines the vegetation of wet trenches with dense herbmoss cover. A detailed description of each subvariant is done. All these syntaxa are compared with the types of mound and trenh communities established previously by the domination principle (Sumina, 1975, 1976, 1979 et al.) and with Brown-Blanquet’ syntaxa published by other authors. The Brown-Blanquet approach in compare with domination principle, clearly demonstrates the similarity between zonal and baidzharakh massifs vegetation. Diagnostic species of syntaxa of baidzharakh vegetation by other authors (Matveyeva, 1994; Zanokha, 1995; Kholod, 2007, 2014; Telyatnikov et al., 2017) differ from ours. On the one hand, this is due to the fact that all mentioned researchers worked in another areas, and on the other, with different hierarchial levels of syntaxa, which are subassociations (or vicariants) in cited works or variants and subvariants in the our. Communities of mounds as well as of trenches in different regions have unlike species composition, but similar apearance, which depends on the similarity of the life form composition and community pattern, stage of their transformation and environmental factors. This fact is a base to group communities by physiognomy in order to have an opportunity of comparative analysis of baidzharakh vegetation diversity in different regions of the Arctic. In total, 6 such groups for thermokarst mounds and trenches are proposed: “tundra-like” ― vegetation of flat polygonal mounds (or trenches) is similar to the plakor (zonal) communities; “eroded tundra-like” ― tundra-like vegetation is presented as fragments, open ground occupies the main part of flat polygonal mounds; “eroded mounds with nonassociated vegetation” ― eroded mounds of various shapes up to sharp conical with absent vegetation at the top and slopes, sparse pioneer vascular plants on a bare substrate and crustose lichens and chionophilous grasses at foots; “meadow-like” ― herb stands with a participation of tundra dwarf-shrubs, mosses, and lichens on elongated smooth-conical mounds and in moderately moist trenches; “communities in snowbeds” ― thin plant cover formed by small mosses, liverworts, crustose lichens, and sparse vascular plants in snowbed habitats on destroyed slightly convex mounds with a lumpy surface and in trenches; “communities of cotton grass” or others, depending on the dominant species ― in wet trenches where vegetation is similar to the arctic hypnum bogs with dominant hygrophyte graminoids as Eriophorum scheuchzeri, E. polystachion, Dupontia fischeri et al. This sheme according to physiognomic features of thermokarst mound and trench communities, as a simplier way to assess the current dynamic stage of the baidzharakh massifs, may be useful for monitoring the thermodenudation activity in different areas of the Arctic, particularly in connection with observed climate changes (ACIA, 2004) and a possible dramatic “cascade of their environmental consequences” (Fraser et al., 2018).


Forests ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 506
Author(s):  
Mayte S. Jiménez-Noriega ◽  
Lauro López-Mata ◽  
Teresa Terrazas

The aims of this study were to evaluate the cambial activity and phenology of three species with different life forms (Alchemilla procumbens, Acaena elongata and Ribes ciliatum) along an altitudinal gradient and to establish which environmental variables (light, soil humidity and temperature) had the greatest influence on cambial activity and phenological stages. Over two years, data on phenology, growth and cambium were gathered every four weeks in three to six sites per species in Sierra Nevada, Mexico. The results showed that Ribes is the only species that terminates cambial activity with leaves senescence and is influenced by the minimum soil temperature. The light environment influenced the vegetative stages in Alchemilla (cryptophyte), while in Acaena (hemicryptophyte), the mean soil temperature explained the findings related to leaf area during the dry season and growth along the gradient. In the three species, the reproductive phase dominated for a longer period at higher elevations, especially in Alchemilla. Only Ribes, the phanerophyte, showed a similar cambial activity to other trees and shrubs. Although cambium reactivates during the dry season, no xylogenesis occurs. The three species varied during the time in which vascular cambium was active, and this was dependent on the altitude. Specifically, the variation was more rhythmic in Ribes and switched on and off in Alchemilla. It is likely that, depending on the life form, vascular cambium may be more or less susceptible to one or more climate factors.


1957 ◽  
Vol 26 (1) ◽  
pp. 37-42 ◽  
Author(s):  
K. KOSUGI ◽  
K. OYOSHI ◽  
A. SUMITOMO ◽  
M. KANEKO

2004 ◽  
Vol 64 (2) ◽  
pp. 201-209 ◽  
Author(s):  
M. A. Batalha ◽  
F. R. Martins

We used Raunkiaer's system to classify in life-forms the vascular plants present in 12 random 25 m² quadrats of a cerrado site. The study area is covered by cerrado sensu stricto and is located in the Valério fragment, at about 22º13'S and 47º51'W, 760 m above sea level, in the Itirapina Ecological and Experimental Station, São Paulo State, southeastern Brazil. The floristic spectrum considers the life-form of each species, while in the frequency spectrum, each species is weighted by its frequency. The vegetation spectrum does not consider the species at all, but only the individuals in each life-form class. In the floristic spectrum, the most represented life-forms were the phanerophytes and the hemicryptophytes, as in other cerrado sites. This spectrum differed significantly from Raunkiaer's normal spectrum, mainly due to under-representation of therophytes and over-representation of phanerophytes. The floristic and frequency spectra were similar, but both differed from the vegetation spectrum. We recommend the floristic spectrum when working at larger scales and a description of the phytoclimate is wanted. The vegetation spectrum is preferable when working at smaller scales and wanting a quantitative description of the physiognomy. The frequency spectrum is not recommended at all.


1970 ◽  
Vol 17 ◽  
pp. 59-68 ◽  
Author(s):  
Susanna Phoboo ◽  
Marcia Da Silva Pinto ◽  
Prasanta C. Bhowmik ◽  
Pramod Kumar Jha ◽  
Kalidas Shetty

Swertia chirayita is an important medicinal plant from Nepal with anti-diabetic, anti-pyretic, anti-malarial and anti-inflammatory potential and used in therapeutic herbal preparations in parts of South Asia. The main phytochemicals in crude aqueous and ethanolic extracts of different plant parts of Swertia chirayita collected from nine different districts of Nepal representing West, East and Central Nepal were quantified using HPLC/DAD (High Performance Liquid Chromatography-Diode Array Detection). The quantities of these phytochemicals were also compared between wild and cultivated plant parts of Swertia chirayita. Amarogentin, mangiferin, swertiamarin were the main phytochemicals in all extracts. The highest quantity of all the three phytochemicals was found in IL (inflorescence and leaf mixture) of all the collected plants samples. There was no significant difference in the amounts of these three phytochemicals between extracts from wild and cultivated plants. The result from this study substantiates the validity of cultivated Swertia chirayita for medicinal purposes and trade.Key words:  Swertia chirayita; HPLC/DAD; Wild; Cultivated; Phytochemicals; Quantification; Mangiferin; Swertiamarin; AmarogentinDOI: 10.3126/eco.v17i0.4118EcoprintAn International Journal of EcologyVol. 17, 2010Page: 59-68Uploaded date: 3 January, 2011


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