scholarly journals Spatial and evolutionary predictability of phytochemical diversity

2021 ◽  
Vol 118 (3) ◽  
pp. e2013344118
Author(s):  
Emmanuel Defossez ◽  
Camille Pitteloud ◽  
Patrice Descombes ◽  
Gaétan Glauser ◽  
Pierre-Marie Allard ◽  
...  

To cope with environmental challenges, plants produce a wide diversity of phytochemicals, which are also the source of numerous medicines. Despite decades of research in chemical ecology, we still lack an understanding of the organization of plant chemical diversity across species and ecosystems. To address this challenge, we hypothesized that molecular diversity is not only related to species diversity, but also constrained by trophic, climatic, and topographical factors. We screened the metabolome of 416 vascular plant species encompassing the entire alpine elevation range and four alpine bioclimatic regions in order to characterize their phytochemical diversity. We show that by coupling phylogenetic information, topographic, edaphic, and climatic variables, we predict phytochemical diversity, and its inherent composition, of plant communities throughout landscape. Spatial mapping of phytochemical diversity further revealed that plant assemblages found in low to midelevation habitats, with more alkaline soils, possessed greater phytochemical diversity, whereas alpine habitats possessed higher phytochemical endemism. Altogether, we present a general tool that can be used for predicting hotspots of phytochemical diversity in the landscape, independently of plant species taxonomic identity. Such an approach offers promising perspectives in both drug discovery programs and conservation efforts worldwide.

2012 ◽  
Vol 65 (4) ◽  
pp. 75-90 ◽  
Author(s):  
Beata Babczyńska-Sendek ◽  
Agnieszka Błońska ◽  
Joanna Hejdysz

The paper presents the results of investigations on the flora of fallow lands on rendzina soils. The research was carried out in the area of the Twardowice Plateau (the Silesian Upland) within 9 areas adjacent to xerothermic grasslands. The investigated flora consisted of 220 vascular plant species with the dominance of native taxa. Plants of xerothermic grasslands and thermophilous edges were the most numerous (32%). The dominance of <em>Libanotis pyrenaica </em>in 4 of the examined areas should be emphasized. The percentage of meadow species was also considerable (25%). Anthropophytes comprised 18% of the flora of fallow lands and archaeophytes prevailed among them (9%). <em>Solidago canadensis</em>, an invasive species, was the constant component of the investigated fallows and sometimes its coverage was remarkable. <br />As a result of the high proportion of xerothermic and thermophilous plants, plants associated with dry soils and soils having an intermediate character between dry and fresh, as well as plants preferring slightly acidic to alkaline soils poor in nitrogen compounds predominated in the investigated fallows. Perennial plants prevailed (65%) in the studied flora and slightly more than half of the species reproduced only by seeds. Competitive plant species (C strategists) had the highest proportion (39%) and species with intermediate strategies CSR, CR and CS were also numerous. <br />The investigations have shown that there are favourable conditions for settling and growth of many xerothermic species in the investigated fallow lands. Moreover, the neighbouring grasslands are the seed source for these areas.


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. 


2021 ◽  
Vol 97 (4) ◽  
Author(s):  
Lucas Dantas Lopes ◽  
Jingjie Hao ◽  
Daniel P Schachtman

ABSTRACT Soil pH is a major factor shaping bulk soil microbial communities. However, it is unclear whether the belowground microbial habitats shaped by plants (e.g. rhizosphere and root endosphere) are also affected by soil pH. We investigated this question by comparing the microbial communities associated with plants growing in neutral and strongly alkaline soils in the Sandhills, which is the largest sand dune complex in the northern hemisphere. Bulk soil, rhizosphere and root endosphere DNA were extracted from multiple plant species and analyzed using 16S rRNA amplicon sequencing. Results showed that rhizosphere, root endosphere and bulk soil microbiomes were different in the contrasting soil pH ranges. The strongest impact of plant species on the belowground microbiomes was in alkaline soils, suggesting a greater selective effect under alkali stress. Evaluation of soil chemical components showed that in addition to soil pH, cation exchange capacity also had a strong impact on shaping bulk soil microbial communities. This study extends our knowledge regarding the importance of pH to microbial ecology showing that root endosphere and rhizosphere microbial communities were also influenced by this soil component, and highlights the important role that plants play particularly in shaping the belowground microbiomes in alkaline soils.


Molecules ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 719
Author(s):  
Meri Yulvianti ◽  
Christian Zidorn

Cyanogenic glycosides are an important and widespread class of plant natural products, which are however structurally less diverse than many other classes of natural products. So far, 112 naturally occurring cyanogenic glycosides have been described in the phytochemical literature. Currently, these unique compounds have been reported from more than 2500 plant species. Natural cyanogenic glycosides show variations regarding both the aglycone and the sugar part of the molecules. The predominant sugar moiety is glucose but many substitution patterns of this glucose moiety exist in nature. Regarding the aglycone moiety, four different basic classes can be distinguished, aliphatic, cyclic, aromatic, and heterocyclic aglycones. Our overview covers all cyanogenic glycosides isolated from plants and includes 33 compounds with a non-cyclic aglycone, 20 cyclopentane derivatives, 55 natural products with an aromatic aglycone, and four dihydropyridone derivatives. In the following sections, we will provide an overview about the chemical diversity known so far and mention the first source from which the respective compounds had been isolated. This review will serve as a first reference for researchers trying to find new cyanogenic glycosides and highlights some gaps in the knowledge about the exact structures of already described compounds.


2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Yamina Micaela Rosas ◽  
Pablo L. Peri ◽  
María Vanessa Lencinas ◽  
Romina Lasagno ◽  
Guillermo J. Martínez Pastur

Abstract Background Biodiversity supports multiple ecosystem services, whereas species loss endangers the provision of many services and affects ecosystem resilience and resistance capacity. The increase of remote sensing techniques allows to estimate biodiversity and ecosystem services supply at the landscape level in areas with low available data (e.g. Southern Patagonia). This paper evaluates the potential biodiversity and how it links with ecosystem services, based on vascular plant species across eight ecological areas. We also evaluated the habitat plant requirements and their relation with natural gradients. A total of 977 plots were used to develop habitat suitability maps based on an environmental niche factor analysis of 15 more important indicator species for each ecological area (n = 53 species) using 40 explanatory variables. Finally, these maps were combined into a single potential biodiversity map, which was linked with environmental variables and ecosystem services supply. For comparisons, data were extracted and compared through analyses of variance. Results The plant habitat requirements varied greatly among the different ecological areas, and it was possible to define groups according to its specialization and marginality indexes. The potential biodiversity map allowed us to detect coldspots in the western mountains and hotspots in southern and eastern areas. Higher biodiversity was associated to higher temperatures and normalized difference vegetation index, while lower biodiversity was related to elevation and rainfall. Potential biodiversity was closely associated with supporting and provisioning ecosystem services in shrublands and grasslands in the humid steppe, while the lowest values were related to cultural ecosystem services in Nothofagus forests. Conclusions The present study showed that plant species present remarkable differences in spatial distributions and ecological requirements, being a useful proxy for potential biodiversity modelling. Potential biodiversity values change across ecological areas allowing to identify hotspots and coldspots, a useful tool for landscape management and conservation strategies. In addition, links with ecosystem services detect potential synergies and trade-offs, where areas with the lowest potential biodiversity are related to cultural ecosystem services (e.g. aesthetic values) and areas with the greatest potential biodiversity showed threats related to productive activities (e.g. livestock).


Polar Record ◽  
2004 ◽  
Vol 40 (3) ◽  
pp. 235-243 ◽  
Author(s):  
J. Whinam ◽  
P.M. Selkirk ◽  
A.J. Downing ◽  
Bruce Hull

Buildings were constructed and artefacts left behind on sub-Antarctic Heard Island, associated with Antarctic research expeditions since 1926. Both bryophytes and vascular plants are colonising many parts of the now derelict buildings. On these structures and artefacts, the authors recorded four species of vascular plants out of the 11 that occur on Heard Island and nine species of mosses out of the 37 recorded from Heard Island. The vascular plant species most frequently recorded colonising structures and artefacts was Pringlea antiscorbutica (288 occurrences), with the area colonised varying from 0.3 cm2 to 430.0 cm2. Muelleriella crassifolia was the moss species that was most frequently recorded (14 occurrences), colonising areas from 2.1 cm2 to 12.9 cm2. The highest number of bryophyte species (seven) was recorded on the stone and cement of the ‘water tank.’ Pringlea antiscorbutica, Poa cookii, Azorella selago, Muelleriella crassifolia, Bryum dichotomum, Dicranoweisia brevipes and Schistidium apocarpum are all expected to continue to colonise the ANARE ruins, as well as areas that have become available since building removal and also possibly areas bared by further deglaciation.


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