Terrestrial and Aquatic Vegetation Diversity of the Pantanal Wetland

Author(s):  
Arnildo Pott ◽  
João Santos Vila da Silva
2011 ◽  
Vol 71 (1 suppl 1) ◽  
pp. 255-263 ◽  
Author(s):  
VJ. Pott ◽  
A. Pott ◽  
LCP. Lima ◽  
SN. Moreira ◽  
AKM. Oliveira

This is a short review of the state of the art concerning diversity of aquatic macrophytes and the main aquatic vegetation types in the Brazilian Pantanal wetland and upper watershed. There are ca. 280 species of aquatic macrophytes on the Pantanal floodplain, with scarce endemism. On the upper watershed, Cerrado wetlands (veredas) and limestone springs have a distinct flora from the Pantanal, with twice the species richness. As a representative case of aquatic habitats influenced by river flood, some primary data are presented for the Pantanal Matogrossense National Park and associated Acurizal Preserve, analysing the floristic similarity among aquatic vegetation types. We comment on problems of conservation and observe that Panicum elephantipes Nees is one of the few natives to compete with the invasive Urochloa arrecta (Hack. ex T. Durand & Schinz) Morrone & Zuloaga.


2015 ◽  
Vol 45 (1) ◽  
pp. 69-84 ◽  
Author(s):  
Rossano Bolpagni ◽  
Andrea Piotti

In the European plains, up to eighty percent of riverine wetlands have been lost due to alteration of hydrological regime and catchment exploitation. This condition is expected to be further negatively exacerbated by climate change. To better understand the observed change in distribution patterns of hydro-hygrophilous vegetation in temperate and Mediterranean floodplains, a vegetation survey was conducted within the lower Oglio River reach in Northern Italy. This river is a mid-size, altered and nutrient-rich left tributary of the Po River. During the 2008 growing season, a total of 60 marginal aquatic habitats were investigated. Overall, 37 vegetation communities were detected, showing a clear predominance of hygrophilous herbaceous plant communities both in terms of representativeness (55.1%) and diversity (54.1%) with respect to woody (22.9% and 10.8%, respectively), and obligate aquatic vegetation (22.0% and 35.1%, respectively). Our main findings were (1) the widespread presence of highly opportunistic, non-native and invasive hygrophilous plant communities (largely dominated by Amorpha fruticosa, Phragmites australis s.l., Amaranthus spp., Bidens spp., and Cyperus spp.), and (2) the limited distribution of hydrophyte vegetation usually dominated by pleustophytes (e.g., Spirodela polyrhiza and Lemna spp.). The present study confirms the dominance of secondary plant communities characterized by the widespread presence of alien species in lowland over-exploited riverscapes, coupled with a low local representativeness of native willow (Salix alba, S. cinerea) communities and anchored macrophyte (batrachid, ceratophyllid, elodeid, myriophyllid) meadows. Total vegetation diversity is consistent with previous studies in similar ecological contexts; on the other hand, at the site scale, the diversity values were extremely low. This is especially true for the aquatic vegetation, and can be related to the high water turbidity and chlorophyll-a concentrations that prevent the establishment and colonization of submerged and rooted hydrophytes. Consequently, we stress the need for metabolic and biogeochemical indicators to assess the actual trophic status of lowland wetlands in order to clarify their potential to be restored.


2006 ◽  
Vol 7 (2) ◽  
pp. 199-209 ◽  
Author(s):  
T. Standovár ◽  
P. Ódor ◽  
R. Aszalós ◽  
L. Gálhidy

2019 ◽  
Vol 5 ◽  
pp. 104
Author(s):  
Suhendra Purnawan ◽  
Subari Yanto ◽  
Ernawati S.Kaseng

This study aims to describe the profile of vegetation diversity in the mangrove ecosystem in Tamuku Village, Bone-Bone-Bone District, North Luwu Regency. This research is a qualitative research using survey methods. The data collection technique uses the Quadrant Line Transect Survey technique. The data analysis technique uses the thinking flow which is divided into three stages, namely describing phenomena, classifying them, and seeing how the concepts that emerge are related to each other. The results of this study are the profile of mangrove vegetation in Tamuku Village, which is still found 16 varieties of true mangrove vegetation and 7 varieties of mangrove vegetation joined in the coastal area of Tamuku Village, Bone-Bone District, North Luwu Regency, South Sulawesi. The condition of mangrove vegetation in Tamuku Village is currently very worrying due to human activities that cause damage such as the project of normalization of flow, opening of new farms, disposal of garbage, water pollution due to chemicals, and exploitation of mangrove forests for living needs. The impact is ecosystem damage and reduced vegetation area as a place to grow and develop mangroves.


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).


2008 ◽  
pp. 68-75 ◽  
Author(s):  
G. S. Taran

In the Ob river floodplain between the mouths of its tributaries Vakh and Tym (within the limits of Aleksandrovskiy district of Tomsk region), phytocoenoses belonging to 9 associations and 2 communities of Braun-Blanquet classification vegetation classes are listed. Class Lemnetea is represented by associations Ricciocarpetum natantis (Segal 1963) Tx. 1974, Lemnetum trisulcae Soó 1927, Stratiotetum aloidis Miljan 1933; class Potametea is done by asso­ciations Potametum perfoliati Koch 1926, Myriophylletum sibirici Taran 1998, Myriophylletum verticillati Soó 1927, Potametum graminei Koch 1926, Potametum pectinati Carstensen 1955, Nymphoidetum peltatae (All. 1922) Bellot 1951, as well as Sagittaria natans and Potamogeton natans—Ceratophyllum demersum communities. The syntaxa distribution in Western Siberia and adjoining territories is characterized.


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