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Sphagnum divinum Flatberg & Hassel. (A) Holotype specimen photo (TRH B-39078), together with the vascular species Andromeda polifolia L., Oxycoccus quadripetalus Gilib., and Sphagnum angustifolium. (B) Topotype specimen photo (TRH B-39080), with mainly green capitula. (C) Typical shoot, specimen from the type locality seen from side. All illustrations are of specimens from the type locality Norway, Sør-Trøndelag county, Klaebu, Oddmyra. Photos: Kjell I. Flatberg.

Sphagnum divinum Flatberg & Hassel. (A) Holotype specimen photo (TRH B-39078), together with the vascular species Andromeda polifolia L., Oxycoccus quadripetalus Gilib., and Sphagnum angustifolium. (B) Topotype specimen photo (TRH B-39080), with mainly green capitula. (C) Typical shoot, specimen from the type locality seen from side. All illustrations are of specimens from the type locality Norway, Sør-Trøndelag county, Klaebu, Oddmyra. Photos: Kjell I. Flatberg.

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Sphagnum magellanicum has been viewed as being a predominantly circumpolar species in the northern hemisphere, but it occurs in the southern hemisphere and was originally described from the southern parts of Chile. It is an ecologically important species in mire ecosystems and has been extensively used as a model to study processes of growth, carbo...

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... (Figure 8) somewhat domed to nearly flat, somewhat to indistinctly 5-radiate from above, varyingly purple-red to wine-red, mottled green and reddish, to sometimes wholly green in shaded habitats, about (15-)20-25(-30) mm in diameter. Capitulum branches (Figure 8) straight to slightly laterally recurved to somewhat incurved, outer branches in side-view somewhat decurved, patent to somewhat erecto-patent in hummock habitats, cylindrical and narrowly tapering with tightly imbricate to somewhat spreading leaves. ...
Context 2
... (Figure 8) somewhat domed to nearly flat, somewhat to indistinctly 5-radiate from above, varyingly purple-red to wine-red, mottled green and reddish, to sometimes wholly green in shaded habitats, about (15-)20-25(-30) mm in diameter. Capitulum branches (Figure 8) straight to slightly laterally recurved to somewhat incurved, outer branches in side-view somewhat decurved, patent to somewhat erecto-patent in hummock habitats, cylindrical and narrowly tapering with tightly imbricate to somewhat spreading leaves. Terminal bud visible, inconspicuous, surrounded by similar-looking, erect, straight, and somewhat longer innermost branches. ...

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Citations

... al. (2001),Thormann et al. (2001),Asada and Warner (2005), Trinder et al. (2008), Breeuwer et al. (2008), Straková et al. (2010), Hagemann and Moroni 140 (2015), Bengtsson et al. (2017),Golovatskaya and Nikonova (2017), andMäkilä et al. (2018). Samples originally classified as Sphagnum magellanicum are here classified as Sphagnum magellanicum aggr.(Hassel et al., 2018). ...
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... H. Klinggr.] as models to assess the importance of abiotic and biotic variables to carbon sequestration in northern peatlands by analysing variation in the growth of these two species across 99 Holarctic peatlands. However, Hassel et al. (2018) provided evidence that plants previously referred to as S. magellanicum in the Northern Hemisphere are in fact two different species (S. divinum Flatberg & K.Hassel and S. medium Limpr.) and that they differ in morphology and ecology. Bengtsson et al. (2020) recognized this taxonomic change and acknowledged that their results may have been affected by the ecological differences between these taxa. ...
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The use of species as a concept is an important metric for assessing biological diversity and ecosystem function. However, delimiting species based on morphological characters can be difficult, especially in aquatic plants that exhibit high levels of variation and overlap. The Sphagnum cuspidatum complex, which includes plants that dominate peatland hollows, provides an example of challenges in species delimitation. Microscopic characters that have been used to define taxa and the possibility that these characters may simply be phenoplastic responses to variation in water availability make species delimitation in this group especially difficult. In particular, the use of leaf shape and serration, which have been used to separate species in the complex, have resulted in divergent taxonomic treatments. Using a combination of high-resolution population genomic data (RADseq) and a robust morphological assessment of plants representing the focal species, we provide evidence to evaluate putative species in this complex. Our data support the recognition of S. cuspidatum, S. fitzgeraldii, S. mississippiense, and S. trinitense as genetically distinct species that can be separated morphologically. These results indicate that S. viride does not differ genetically from S. cuspidatum. Our results are broadly relevant to other aquatic groups where leaf shape and marginal teeth are used to distinguish species.
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Functional traits are a set of characteristics that are expressed in the phenotype of an individual organism as a response to the environment and their impact on the ecosystem’s properties. They are positioned at the crossroads between the response and influence of the organisms, creating a certain interest in functional ecological and evolutionary fields. Due to this unique position, they are divided into two categories: effect functional traits and response functional traits. Effect traits describe the influence of the species on the environment regardless of whether such traits are an adaptive advantage to the individual or not. In Bryophyta, one of the most important effect traits is water holding capacity (WHC), which is their means of regulating ecosystem hydrology. On a global scale, mosses’ WHC is manifested in the slowdown of the large water cycle, in the storage of huge volumes of fresh water by peatlands and in the enormous paludification of Western Siberia. The main goal of our research was to obtain the water holding capacity measurements of tundra and taiga moss species to establish the base and foundation for environmental monitoring in the north of Siberia—the region with the most rapidly changing climate. Both the capacity to hold water within the moss tissues (WHC) and the capacity to hold water externally between the morphological structures (leaves, branches, rhizoids, etc.) (WHCe) were measured. In total, 95 samples of 9 Sphagnum and 5 true mosses species were involved to the research; some species were collected at two or three sampling sites within two natural zones/subzones that gave us the opportunity to compare the WHC along the meridional transection. In average, the northern taiga samples showed slightly higher WHC than tundra samples, probably due to the environmental specifics of the habitat—the taiga habitats were more moist, while the tundra was drier. Overall, in the majority of species, the standard deviation calculation revealed that the variability of WHCe is significantly higher than that of WHC. Such high variability in WHCe may be explained in regard to the morphological features of each individual considerably shifting between the samples of the same species while the anatomical features retain more stable results.
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We present a first complete overview of the bryophyte-lichen syntaxa in the Netherlands, including diagnostic species and Red List status of vegetations representing each (sub)association. The classification is based on more than 5000 Dutch vegetation relevés, the majority recorded after the year 2000. Whenever appropriate, we integrated bryophyte and lichen syntaxonomy. The Dutch list of bryolichenosociological units consists of 168 syntaxa: 16 classes, 27 orders, 37 alliances, 82 associations and 6 subassociations. We present synoptic tables of 13 newly described syntaxa: two alliances, nine associations and two subassociations. Finally, we present ranges of the abiotic habitat variables moisture, light availabilty, nutrient richness and acidity on class level, based on estimated values of diagnostic species of individual associations in each class.
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