scholarly journals Reintroduction of fen plant communities on a degraded minerotrophic peatland

Botany ◽  
2016 ◽  
Vol 94 (11) ◽  
pp. 1041-1051 ◽  
Author(s):  
Line Rochefort ◽  
Marie-Claire LeBlanc ◽  
Vicky Bérubé ◽  
Sandrine Hugron ◽  
Stéphanie Boudreau ◽  
...  

We have developed an approach to restore bogs after peat extraction, but, when sedge-peat layers are exposed, the minerotrophic remnant peat conditions require restoration towards a fen ecosystem. Three restoration techniques, all including rewetting actions, were tested to assist fen vegetation recovery. None of the restoration techniques were effective at establishing fen bryophytes. However, for vascular plants, two techniques gave promising results in terms of species composition, although the vascular plant cover remained lower than in the reference fens. Depending on the site conditions, we suggest applying two restoration techniques to restore peatlands in areas of exposed sedge peat. In areas where sparse cover of fen species may have spontaneously established, rewetting should be carried out to raise water levels and create favourable conditions for their expansion. In areas covered with undesirable species or with inadequate topography for rewetting, surface peat should be remodeled and vegetation introduced. Since mechanized diaspore transfer did not result in a satisfactory cover of fen plants, other means of introduction could be considered, alone or in combination. A complementary fertilization experiment showed that fertilization with phosphorus could be an effective solution to enhance the establishment of mechanically introduced plant diaspores.

2018 ◽  
pp. 149-154

Vera Antonovna Martynenko (17.02.1936–06.01.2018) — famous specialist in the field of studying vascular plant flora and vegetation of the Far North, the Honored worker of the Komi Republic (2006), The Komi Republic State Scientific Award winner (2000). She was born in the town Likhoslavl of the Kali­nin (Tver) region. In 1959, Vera Antonovna graduated from the faculty of soil and biology of the Leningrad State University and then moved to the Komi Branch of USSR Academy of Science (Syktyvkar). From 1969 to 1973 she passed correspondence postgraduate courses of the Komi Branch of USSR Academy of ­Science. In 1974, she received the degree of candidate of biology (PhD) by the theme «Comparative analysis of the boreal flora at the Northeast European USSR» in the Botanical Institute (St. Petersburg). In 1996, Vera Antonovna received the degree of doctor of biology in the Institute of plant and animal ecology (Ekaterinburg) «Flora of the northern and mid subzones of the taiga of the European North-East». The study and conservation of species and coenotical diversity of the plant world, namely the vascular plants flora of the Komi Republic and revealing its transformation under the anthropogenic influence, was in the field of V. A. Martynenko’ scientific interests. She made great contribution to the study of the Komi Republic meadow flora and the pool of medi­cinal plants. She performed inventorying and mapping the meadows of several agricultural enterprises of the Republic, revealed the species composition and places for harvesting medicinal plants and studied their productivity in the natural flora of the boreal zone. The results of her long-term studies were used for making the NPA system and the Red Book of the Komi Republic (1998 and 2009). Vera Antonovna participated in the research of the influence of placer gold mining and oil development on the natural ecosystems of the North, and developed the method of long-term monitoring of plant cover. Results of these works are of high practical value. V. A. Martynenko is an author and coauthor of more than 130 scientific publications. The most important jnes are «Flora of Northeast European USSR» (1974, 1976, and 1977), «Floristic composition of fodder lands of the Northeast Europe» (1989), «The forests of the Komi Republic» (1999), «Forestry of forest resources of the Komi Republic» (2000), «The list of flora of the Yugyd va national park» (2003), «The guide for vascular plants of the Syktyvkar and its vicinities» (2005), «Vascular plants of the Komi Republic» (2008), and «Resources of the natural flora of the Komi Republic» (2014). She also was an author of «Encyclopedia of the Komi Republic» (1997, 1999, and 2000), «Historical and cultural atlas of the Komi Republic» (1997), «Atlas of the Komi Republic» (2001, 2011). V. A. Martynenko made a great contribution to the development of the botanical investigations in the North. Since 1982, during more than 10 years, she was the head of the Department of the Institute of Biology. Three Ph. D. theses have been completed under her leadership. Many years, she worked actively in the Dissertation Council of the Institute of biology Komi Scientific Centre UrB RAS.  The death of Vera Antonovna Martynenko is a heavy and irretrievable loss for the staff of the Institute of Biology. The memory of Vera Antonovna will live in her numerous scientific works, the hearts of students and colleagues.


1999 ◽  
Vol 47 (1) ◽  
pp. 49-59 ◽  
Author(s):  
Eviatar Nevo ◽  
Ori Fragman ◽  
Amots Dafni ◽  
Avigdor Beiles

Species diversity of plants was recorded in 1992 and 1993 at seven stations of the “Evolution Canyon” microsite. Higher solar radiation on the South-Facing Slope (SFS) causes warm, xeric savannoid formation versus temperate, cool, mesic, dense maquis on the North-Facing Slope (NFS), and riverine, segetal plant formations on the Valley Bottom (VB). In an area of 7000 m2, we recorded 320 vascular plant species in 217 genera and 59 families. Plant cover varied from 35% (SFS) to 150% (NFS). Annuals predominated among all life forms (61.3% of all species). SFS and NFS varied in species content, sharing only 31–18% of species. Phytogeographical types varied among the two slopes and valley bottom. Inter-and intraslope species composition varied drastically due to differential microclimatic stresses, thereby demonstrating at a microscale natural selection in action.


Soil Research ◽  
1994 ◽  
Vol 32 (3) ◽  
pp. 389 ◽  
Author(s):  
DJ Eldridge ◽  
RSB Greene

Microbiotic crusts are assemblages of non-vascular plants (mosses, liverworts, algae, lichens, fungi, bacteria and cyanobacteria) which form intimate associations with surface soils. They play a major role in infiltration processes through changes to soil physico-chemical properties, and through their influence on soil surface roughness. Whilst some research suggests that they may restrict infiltration, Australian experience is that they are generally associated with enhanced infiltration. Unlike physical soil crusts, microbiotic crusts stabilize the soil against water and wind erosion, increasing landscape stability, particularly in areas of low vascular plant cover. Microbiotic crusts are thus useful indicators of soil surface condition, and cyanobacteria in the crusts fix nitrogen which may be utilized by developing vascular plant seedlings. Little is known, however, about how they interact with vascular plants and soil invertebrates. Their role in rangeland ecosystems has received renewed attention over the past few years with an increasing interest in ecologically sustainable development of arid and semi-arid grazing systems. In this review we discuss the characteristics and distribution of microbiotic crusts in the rangelands of Australia, their roles in soil and ecological processes and the impacts of fire and grazing. Finally we propose a new system for classifying crusts into functional groups and identify areas requiring further investigation.


1978 ◽  
Vol 56 (20) ◽  
pp. 2470-2490 ◽  
Author(s):  
Katherine L. Bell ◽  
L. C. Bliss

Within the northwestern islands of the High Arctic, the vegetation and flora of King Christian Island are very representative. Five plant communities were recognized in a moisture gradient from a moss–rush moist meadow with 22 species of vascular plants and 13% cover (total plant cover 93%) to lichen barrens on low ridges with 8 species of vascular plants and 3% cover (total plant cover 24%). Root systems of 30 of the 34 known vascular plant species were examined. Root:shoot ratios (alive) are generally 0.2 to 0.7. Roots are estimated to live 1.5 years in Phippsia algida, 3.4–3.7 years in Alopecurus alpinus and Puccinellia vaginata, and 7–13 years in Luzula nivalis, L. confuse), and Cerastium arcticum. Optimal root growth occurs at 12 to 20 °C but cold field soils (1 to 3 °C) reduce these rates by 90%. Root growth was also reduced by low soil water potentials (< − 14 bars (1 bar = 100 kPa)), conditions seldom encountered in these sites. Limited root growth due to cold soils is combined with the adaptive advantages of small roots to produce small plants and sparse cover in these polar semidesert lands.


2021 ◽  
Vol 118 (25) ◽  
pp. e2004192118
Author(s):  
Rachel M. Wilson ◽  
Malak M. Tfaily ◽  
Max Kolton ◽  
Eric R. Johnston ◽  
Caitlin Petro ◽  
...  

In this study, a suite of complementary environmental geochemical analyses, including NMR and gas chromatography-mass spectrometry (GC-MS) analyses of central metabolites, Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) of secondary metabolites, and lipidomics, was used to investigate the influence of organic matter (OM) quality on the heterotrophic microbial mechanisms controlling peatland CO2, CH4, and CO2:CH4 porewater production ratios in response to climate warming. Our investigations leverage the Spruce and Peatland Responses under Changing Environments (SPRUCE) experiment, where air and peat warming were combined in a whole-ecosystem warming treatment. We hypothesized that warming would enhance the production of plant-derived metabolites, resulting in increased labile OM inputs to the surface peat, thereby enhancing microbial activity and greenhouse gas production. Because shallow peat is most susceptible to enhanced warming, increases in labile OM inputs to the surface, in particular, are likely to result in significant changes to CO2 and CH4 dynamics and methanogenic pathways. In support of this hypothesis, significant correlations were observed between metabolites and temperature consistent with increased availability of labile substrates, which may stimulate more rapid turnover of microbial proteins. An increase in the abundance of methanogenic genes in response to the increase in the abundance of labile substrates was accompanied by a shift toward acetoclastic and methylotrophic methanogenesis. Our results suggest that as peatland vegetation trends toward increasing vascular plant cover with warming, we can expect a concomitant shift toward increasingly methanogenic conditions and amplified climate–peatland feedbacks.


There is evidence, although inconclusive, that a biologically active soil cover existed long before the late Silurian. The earliest vascular plants may have colonized a land surface containing well-developed soils which were functioning biologically and biochemically in similar ways to modern soils. In any discussion of the late Silurian-early Devonian ‘invasion of the land’, two basic questions arise in relation to the history of the land cover and its soils: (i) Did vascular plants colonize a barren landscape or did biologically functioning soils already exist? (ii) What changes did the vascular plant cover cause to the land surface and its soils? This latter question has been tackled by Retallack (this symposium) and the following is a discussion of some aspects of the former. Many soil-forming processes are purely physical or physico-chemical in origin and examples of such pedogenic modifications of the land surface have now been documented from the Precambrian and lower Palaeozoic (Retallack 1981). However, there is also some evidence that these early soils were biologically active and were associated with microbial communities. Golubic & Campbell (1979) have compared the mid Precambrian microfossil, Eosynechnococcus moorei Hofmann with the extant cyanobacterium Gloeothece coerulea Geitler, which is a subaerial form. They have suggested that prokaryotic communities may have colonized the land surface as long ago as the early Precambrian. Organic-rich palaeosols are known from Blind River Formation of Ontario (Campbell 1979) which is 2.4 Ga old.


2017 ◽  
Vol 28 (1-2) ◽  
pp. 28-35 ◽  
Author(s):  
B. A. Baranovski

Nowadays, bioecological characteristics of species are the basis for flora and vegetation studying on the different levels. Bioecological characteristics of species is required in process of flora studying on the different levels such as biotopes or phytocenoses, floras of particular areas (floras of ecologically homogeneous habitats), and floras of certain territories. Ramensky scale is the one of first detailed ecological scales on plant species ordination in relation to various environmental factors; it developed in 1938 (Ramensky, 1971). A little later (1941), Pogrebnyak’s scale of forest stands was proposed. Ellenberg’s system developed in 1950 (Ellenberg, 1979) and Tsyganov’s system (Tsyganov, 1975) are best known as the systems of ecological scales on vascular plant species; these systems represent of habitat detection by ecotopic ecomorphs of plant species (phytoindication). Basically, the system proposed by Alexander Lyutsianovich Belgard was the one of first system of plant species that identiified ectomorphs in relation to environmental factors. As early as 1950, Belgard developed the tabulated system of ecomorphs using the Latin ecomorphs abbreviation; he also used the terminology proposed in the late 19th century by Dekandol (1956) and Warming (1903), as well as terminology of other authors. The article analyzes the features of Belgard’s system of ecomorphs on vascular plants. It has certain significance and advantages over other systems of ecomorphs. The use of abbreviated Latin names of ecomorphs in tabular form enables the use shortened form of ones. In the working scheme of Belgard’s system of ecomorphs relation of species to environmental factors are represented in the abbreviated Latin alphabetic version (Belgard, 1950). Combined into table, the ecomorphic analysis of plant species within association (ecological certification of species), biotope or area site (water area) gives an explicit pattern on ecological structure of flora within surveyed community, biotope or landscape, and on environmental conditions. Development and application by Belgrard the cenomorphs as «species’ adaptation to phytocenosis as a whole» were completely new in the development of systems of ecomorphs and, in this connection, different coenomorphs were distinguished. Like any concept, the system of ecomorphs by Belgard has the possibility and necessity to be developed and added. Long-time researches and analysis of literature sources allow to propose a new coenomorph in the context of Belgard’s system of ecomorphs development: silvomargoant (species of forest margin, from the Latin words margo – edge, boundary (Dvoretsky, 1976), margo – margin, ad margins silvarum – along the deciduous forest margins). As an example of ecomorphic characterization of species according to the system of ecomorphs by Belgard (when the abbreviated Latin ecomorph names are used in tabular form and the proposed cenomorph is used), it was given the part of the table on vascular plants ecomorphs in the National Nature Park «Orelsky» (Baranovsky et al). The Belgard’s system of ecomorphs is particularly convenient and can be successfully applied to data processing in the ecological analysis of the flora on wide areas with significant species richness, and the proposed ecomorph will be another necessary element in the Belgard’s system of ecomorphs. 


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).


Author(s):  
L. E. Ryff

The aim of the work is to supplement and clarify the annotated list of vascular plants of “Castel” nature reserve on the Southern coast of the Crimea. Methods. The work is based on the results of long standing field research, which was carried out by the traditional route-reconnaissance method, analysis of YALT herbarium materials and data from literary and Internet sources. Arealogical and biomorphological characteristics of species are given according to "Biological Flora of the Crimea" by V.N. Golubev, biotope coding according to EUNIS habitat classification. The nomenclature of taxa corresponds to the " Spontaneuos flora of the Crimean peninsula" by A.V. Yena and to international databases Euro+Med PlantBase, The Plant List, Catalog of Life. Results. An additional annotated list of vascular plants of “Castel” nature reserve has been compiled, including 152 species, subspecies and cultivars from 97 genera of 38 families, of which 53 genera and 11 families have also not been cited for this territory before. Arealogical, biomorphological, biotopic and sozological characteristics of the taxa are given. As a result of a critical analysis of the list previously published by E.S. Krainyuk, four species were redefined, two species were proposed to be excluded from the flora of the specially protected natural area, several taxa are considered doubtful. Conclusions. The list of vascular plant taxa in “Castel” nature reserve has been supplemented with 11 families, 53 genera, and 152 species, subspecies, and cultivars; several species from the previously compiled list have been proposed to be excluded or considered doubtful. Thus, the flora of the protected area includes at least 425 species from 68 families. For the first time, the biotopic characteristic of the flora of the reserve was established.


Wetlands ◽  
2021 ◽  
Vol 41 (6) ◽  
Author(s):  
Alba Cuena-Lombraña ◽  
Mauro Fois ◽  
Annalena Cogoni ◽  
Gianluigi Bacchetta

AbstractPlants are key elements of wetlands due to their evolutionary strategies for coping with life in a water-saturated environment, providing the basis for supporting nearly all wetland biota and habitat structure for other taxonomic groups. Sardinia, the second largest island of the Mediterranean Basin, hosts a great variety of wetlands, of which 16 are included in eight Ramsar sites. The 119 hydro- and hygrophilous vascular plant taxa from Sardinia represent the 42.6% and 37.9% of the number estimated for Italy and Europe, respectively. Moreover, around 30% of Sardinia’s bryological flora, which is made up of 498 taxa, is present in temporary ponds. An overview at regional scale considering algae is not available, to our knowledge, even though several specific studies have contributed to their knowledge. In order to find the most investigated research themes and wetland types, identify knowledge gaps and suggest recommendations for further research, we present a first attempt to outline the work that has been hitherto done on plants in lentic habitats in Sardinia. Three plant groups (algae, bryophytes and vascular plants), and five research themes (conservation, ecology, inventory, palaeobotany and taxonomy) were considered. After a literature review, we retained 202 papers published from 1960 to 2019. We found that studies on vascular plants, as plant group, were disproportionately more numerous, and inventories and ecology were the most investigated research themes. Although efforts have recently been made to fill these long-lasting gaps, there is a need for updating the existing information through innovative methods and integrative approaches.


Sign in / Sign up

Export Citation Format

Share Document