Academic literature on the topic 'Bryophytes – Classification'

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Journal articles on the topic "Bryophytes – Classification"

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Кучеров, Илья Борисович, Галина Александровна Гришуткина, Виктория Владимировна Телеганова, and Алексей Дмитриевич Потемкин. "On the diagnostic potential of epiphytic bryophytes in forest vegetation classification." Herald of Tver State University. Series: Biology and Ecology, no. 1(61) (April 13, 2021): 102–23. http://dx.doi.org/10.26456/vtbio189.

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Эпифитные и эпиксильные виды мохообразных и лишайников могут выступать в качестве диагностических не только при дифференциации своих синузий, но и на уровне лесного сообщества в целом, формируя единые детерминантные группы вместе с сосудистыми растениями и эпигейными мхами. Это подтверждают результаты доминантно-детерминантной классификации широколиственных лесов, описанных в заповедниках «Калужские засеки» и «Мордовский». В обоих случаях выделенные синтаксоны поддаются флористической дифференциации с помощью не только сосудистых растений, но и эпифитных мохообразных. При необходимости их можно было бы разграничить исключительно по видам эпифитной бриосинузии. Формирование единых детерминантных групп обусловлено влиянием факторов, единообразно воздействующих на все виды, входящие в эти группы. Первостепенную роль предположительно играют микроклиматические факторы, особенно влажность и амплитуды температур приземного слоя воздуха. Эдафические факторы не оказывают прямого влияния на сопряженность видов сосудистых растений и эпифитных мохообразных, но их косвенное влияние также может быть существенным. Piphytic and epixylic species of bryophytes and lichens may serve as determinants in differentiation of not only their synusiae but also at the level of forest plant communities where they grow, forming integrated differential groups together with vascular plant and epigeic bryophyte species. This is proved by the results of the broadleaved forest classification, performed following the complex dominant-determinant approach in the Kaluzhskie Zaseki (see Table 1) and Mordovian (see Table 2) nature reserves, Russia. All the recognized broadleaved-forest syntaxa are subject to distinct floristic differentiation with the help of both vascular and epiphytic bryophyte species under ecologically contrasting habitat conditions. Moreover, if necessary, these syntaxa can be distinguished using the epiphytic species only. The ecological and phytocoenotical association of vascular and epiphytic bryophyte species presumably originates due to microclimatic factors such as air humidity and temperature ranges near the ground. Edaphic factors do not influence the association of vasculars and epiphytic bryophytes within the integrated determinant groups directly, but their indirect influence may be also essential.
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Peters, Treutler, Döll, Kindt, Hankemeier, and Neumann. "Chemical Diversity and Classification of Secondary Metabolites in Nine Bryophyte Species." Metabolites 9, no. 10 (2019): 222. http://dx.doi.org/10.3390/metabo9100222.

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The central aim in ecometabolomics and chemical ecology is to pinpoint chemical features that explain molecular functioning. The greatest challenge is the identification of compounds due to the lack of constitutive reference spectra, the large number of completely unknown compounds, and bioinformatic methods to analyze the big data. In this study we present an interdisciplinary methodological framework that extends ultra-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry (UPLC/ESI-QTOF-MS) with data-dependent acquisition (DDA-MS) and the automated in silico classification of fragment peaks into compound classes. We synthesize findings from a prior study that explored the influence of seasonal variations on the chemodiversity of secondary metabolites in nine bryophyte species. Here we reuse and extend the representative dataset with DDA-MS data. Hierarchical clustering, heatmaps, dbRDA, and ANOVA with post-hoc Tukey HSD were used to determine relationships of the study factors species, seasons, and ecological characteristics. The tested bryophytes showed species-specific metabolic responses to seasonal variations (50% vs. 5% of explained variation). Marchantia polymorpha, Plagiomnium undulatum, and Polytrichum strictum were biochemically most diverse and unique. Flavonoids and sesquiterpenoids were upregulated in all bryophytes in the growing seasons. We identified ecological functioning of compound classes indicating light protection (flavonoids), biotic and pathogen interactions (sesquiterpenoids, flavonoids), low temperature and desiccation tolerance (glycosides, sesquiterpenoids, anthocyanins, lactones), and moss growth supporting anatomic structures (few methoxyphenols and cinnamic acids as part of proto-lignin constituents). The reusable bioinformatic framework of this study can differentiate species based on automated compound classification. Our study allows detailed insights into the ecological roles of biochemical constituents of bryophytes with regard to seasonal variations. We demonstrate that compound classification can be improved with adding constitutive reference spectra to existing spectral libraries. We also show that generalization on compound classes improves our understanding of molecular ecological functioning and can be used to generate new research hypotheses.
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Newmaster, Steven G., René J. Belland, André Arsenault, and Dale H. Vitt. "Patterns of bryophyte diversity in humid coastal and inland cedar–hemlock forests of British Columbia." Environmental Reviews 11, S1 (2003): S159—S185. http://dx.doi.org/10.1139/a03-016.

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Mosses and hepatics (bryophytes) are the most diverse and abundant understorey vegetation within the Coastal Western Hemlock (CWH) and Interior Cedar–Hemlock (ICH) zones of British Columbia. This study intensively sampled bryophytes in 287 young- and old-growth stands in the CWH and ICH zones. Two major variables strongly influence the patterning of bryophyte diversity in these zones: stand age and habitat heterogeneity. Canonical correspondence analyses (CCA) identified these as the most important variables explaining stand–environment interactions. Alpha diversity is much greater in old-growth forests and beta diversity is high between young and old forests. Old-growth cedar–hemlock forests have between 60 (ICH) and 100% (CWH) more species than younger forests disturbed by wildfire in the ICH zones or logging in the CWH zones. Furthermore, a stand classification built on species composition partitioned species into stands of different ages and mesohabitat heterogeneity. Beta diversity was also partitioned between stands of different ages and habitat heterogeneity. This indicates that both young and old forests have a unique assemblage of species. Indicator analysis was used to choose a partial lists of species that are indicators of "old growthness". These old forests support a rich flora of hepatics and rare western North American endemics. High environmental continuity is associated with the most humid watersheds and cedar–hemlock forests within these watersheds have the highest bryophyte diversity. The establishment of rich communities of bryophytes in the moist cedar–hemlock forest has been occurring over the last 2000–7000 years, with the coastal rainforest much older than the inland rainforest. Large-scale disturbance, such as forestry, threatens the existence of these highly diverse communities. A better understanding of the patterning of bryophyte diversity will provide an opportunity to minimize the impact of forest operations on biodiversity. Bryophyte diversity in British Columbia cedar–hemlock forests will be sustained through ecosystem management of old-growth legacies (i.e., landscapes, stands, and their components) and preservation of areas of high diversity. Temporal and habitat variables are influential in the patterning of bryophyte diversity. Management plans that consider these variables will be better equipped to manage cedar–hemlock forests for maintaining biodiversity. Key words: biodiversity, bryophytes, cedar–hemlock, CWH, disturbance, ecosystem management, floristic habitat sampling, forest conservation, ICH, old growth, patterning of diversity, rare species, species richness.
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Harris, Eric S. J. "Ethnobryology: traditional uses and folk classification of bryophytes." Bryologist 111, no. 2 (2008): 169–217. http://dx.doi.org/10.1639/0007-2745(2008)111[169:etuafc]2.0.co;2.

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Maksimova, Viktorija, Laura Klavina, Oskars Bikovens, Andris Zicmanis, and Oskars Purmalis. "Structural Characterization and Chemical Classification of Some Bryophytes Found in Latvia." Chemistry & Biodiversity 10, no. 7 (2013): 1284–94. http://dx.doi.org/10.1002/cbdv.201300014.

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Troitsky, A. V., M. S. Ignatov, V. K. Bobrova, and I. A. Milyutina. "Contribution of genosystematics to current concepts of phylogeny and classification of bryophytes." Biochemistry (Moscow) 72, no. 12 (2007): 1368–76. http://dx.doi.org/10.1134/s0006297907120115.

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Peters, Kristian, Gerd Balcke, Niklas Kleinenkuhnen, Hendrik Treutler, and Steffen Neumann. "Untargeted In Silico Compound Classification—A Novel Metabolomics Method to Assess the Chemodiversity in Bryophytes." International Journal of Molecular Sciences 22, no. 6 (2021): 3251. http://dx.doi.org/10.3390/ijms22063251.

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In plant ecology, biochemical analyses of bryophytes and vascular plants are often conducted on dried herbarium specimen as species typically grow in distant and inaccessible locations. Here, we present an automated in silico compound classification framework to annotate metabolites using an untargeted data independent acquisition (DIA)–LC/MS–QToF-sequential windowed acquisition of all theoretical fragment ion mass spectra (SWATH) ecometabolomics analytical method. We perform a comparative investigation of the chemical diversity at the global level and the composition of metabolite families in ten different species of bryophytes using fresh samples collected on-site and dried specimen stored in a herbarium for half a year. Shannon and Pielou’s diversity indices, hierarchical clustering analysis (HCA), sparse partial least squares discriminant analysis (sPLS-DA), distance-based redundancy analysis (dbRDA), ANOVA with post-hoc Tukey honestly significant difference (HSD) test, and the Fisher’s exact test were used to determine differences in the richness and composition of metabolite families, with regard to herbarium conditions, ecological characteristics, and species. We functionally annotated metabolite families to biochemical processes related to the structural integrity of membranes and cell walls (proto-lignin, glycerophospholipids, carbohydrates), chemical defense (polyphenols, steroids), reactive oxygen species (ROS) protection (alkaloids, amino acids, flavonoids), nutrition (nitrogen- and phosphate-containing glycerophospholipids), and photosynthesis. Changes in the composition of metabolite families also explained variance related to ecological functioning like physiological adaptations of bryophytes to dry environments (proteins, peptides, flavonoids, terpenes), light availability (flavonoids, terpenes, carbohydrates), temperature (flavonoids), and biotic interactions (steroids, terpenes). The results from this study allow to construct chemical traits that can be attributed to biogeochemistry, habitat conditions, environmental changes and biotic interactions. Our classification framework accelerates the complex annotation process in metabolomics and can be used to simplify biochemical patterns. We show that compound classification is a powerful tool that allows to explore relationships in both molecular biology by “zooming in” and in ecology by “zooming out”. The insights revealed by our framework allow to construct new research hypotheses and to enable detailed follow-up studies.
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Ievinsh, Gederts, Laura Gaile, Didzis Elferts, and Ligita Liepiņa. "Relationship Between Functional Traits, Functional Types, and Habitat in Boreonemoral Bryophytes." Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences. 74, no. 3 (2020): 196–205. http://dx.doi.org/10.2478/prolas-2020-0031.

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AbstractThe aim of the present study was to determine a relationship between physiological traits and functional types of bryophytes from five boreonemoral habitats with a particular emphasis on discriminative ability of these traits. Sampling of 25 species was performed four times during one season. Water content, chlorophyll a fluorescence and photosynthetic pigment concentration were measured in field and water-equilibrated samples. Principal component analysis indicated the existence of an inverse relationship between concentration of pigments and water content. Linear discriminant analysis showed that relatively high mean predicted posterior probabilities of correct classification of functional types by physiological traits were found for water conducting system, followed by substrate and habitat, but it was highly variable and type-specific for life form and relatively less variable for life strategy. Field water content had the highest average discriminative importance among physiological traits, followed by chlorophyll fluorescence indices field Fv/Fm, equilibrated PI, equilibrated RC/ABS, and field RC/ABS. Photosynthetic pigment concentrations had relatively less average importance for classification of functional types.
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Forbes, Bruce C. "The importance of bryophytes in the classification of human-disturbed high arctic vegetation." Journal of Vegetation Science 5, no. 6 (1994): 877–84. http://dx.doi.org/10.2307/3236200.

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Kürschner, Harald. "Wissenschaftliche Ergebnisse der BRYOTROP-Expedition nach Zaire und Rwanda 5. Höhengliederung epiphytischer Moose im östlichen Kongobecken und den angrenzenden Gebirgsstöcken (Parc National de Kahuzi-Biega/Zaire, Forêt de Nyungwe/Rwanda)." Bryophyte Diversity and Evolution 11, no. 1 (1995): 77–85. http://dx.doi.org/10.11646/bde.11.1.5.

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By mean of a line-taxation (ordination), the floristic discontinuities of epiphytic bryophytes were shown within an altitudinal gradient from the eastern Congo basin to the mountains of the Riftvalley (Mt. Kahuzi) (BRYOTROP III-transect). By this ordination, the epiphytic vegetation can be grouped into four ecological groups, indicating the climatic factors. They show a strong correlation to the known altitudinal zonation, the different forest zones, and the plantsociological classification. These groups consist of taxa of different relationships which grow and evolve under similar environmental conditions.
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Dissertations / Theses on the topic "Bryophytes – Classification"

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Zhang, Li, and 張力. "Diversity and conservation of Hong Kong bryophytes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2001. http://hub.hku.hk/bib/B30138103.

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Hagemann, Ulrike. "Bryophyte-regulated deadwood and carbon cycling in humid boreal forests." Doctoral thesis, 2010. https://tud.qucosa.de/id/qucosa%3A25489.

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The presented thesis investigates the role of bryophytes in the deadwood and carbon (C) cycle of boreal black spruce forests in Labrador, Canada. All major forest C pools (live-tree, standing and downed deadwood, organic layer, mineral soil) were quantified for three old-growth, nine clearcut harvested, and three burned forest stands in order to characterize forest C dynamics of a high-latitude humid boreal forest ecosystem. Tree and aboveground deadwood C dynamics of Labrador black spruce forests were similar to those of drier or warmer boreal forests. However, due to bryophyte-driven processes such as woody debris (WD) burial and paludification, the studied forests contained high organic layer, mineral soil, and buried wood C stocks. The comprehensive field-measured data on C stocks was used to evaluate the CBM-CFS3, a Canadian national-scale C budget model, with respect to its applicability to Labrador black spruce and humid boreal forests elsewhere. After selected biomass estimation and deadwood decay parameters had been adjusted, the CBM-CFS3 represented measured live-tree and aboveground deadwood C dynamics well. The CBM-CFS3 was initially designed for well-drained upland forests and does not reflect processes associated with bryophytes and high forest floor moisture content, thus not capturing the large amounts of buried wood and mineral soil C observed in the studied forests. Suggestions are made for structural changes to the CBM-CFS3 and other forest ecosystem C models to more adequately represent the bryophyte-regulated accumulation of buried wood, organic layer, and mineral soil C. Accuracy of forest C models could be further improved by differentiating WD decomposition rates by disturbance history, because WD respiration reflects disturbance-induced changes in temperature and moisture regimes. In Labrador, WD respiration was limited by low WD moisture levels and high temperatures in burned stands, and by high WD moisture contents and low temperatures in old-growth stands. Following harvesting, residual vegetation prevents the desiccation of WD, resulting in significantly higher WD respiration compared to old-growth and burned stands. Moreover, the bryophyte layer recovers faster following harvest than following fire, which reduces WD desiccation due to moisture retention, water transfer, and moisture-induced cooling and results in higher WD decomposition rates. Bryophytes are thus a key driver of the deadwood and C cycle of humid boreal Labrador black spruce forests. The author recommends to classify these and similar boreal forests as a functional ecosystem group called “humid boreal forests”, preliminarily defined as “boreal forest ecosystems featuring a bryophyte-dominated ground vegetation layer associated with low soil temperatures, high moisture levels, low dead organic matter decomposition rates, and subsequently (in the absence of stand-replacing disturbances) an accumulation of buried wood embedded in a thick organic layer”. Bryophytes are also an integral component of many coniferous forests outside the boreal biome. Bryophyte-regulated processes such as WD burial or paludification are thus likely significant to the global C cycle. The potential climate change-induced release of large amounts of CO2 from buried wood and soil C pools necessitates an increased understanding of how bryophyte productivity and decomposition constraints will change with increasing temperature and varying moisture regimes. Ecosystems such as humid boreal forests with potentially high C losses to the atmosphere may thus be identified and counteractive forest management strategies can be developed and implemented.<br>Cette thèse de doctorat s’intéresse à l’influence qu’exercent les mousses sur les cycles du bois mort et du carbone (C) dans des pessières noires boréales humides du Labrador, Canada. Toutes les réservoirs majeurs de C (arbres vivants, bois mort sur pied et effondré, l’horizon de matière organique, sol minéral) de trois pessières vierges, neuf coupes à blanc et de trois pessières brûlées ont été quantifiés pour caractériser le cycle du C des forêts humides boréales du nord. Les dynamismes de C des arbres vivants et du bois mort supraterrestre ressemblaient à ceux des forêts boréales plus sèches ou aux températures plus chaudes. À cause des processus régulés par les mousses (l’enterrement du bois mort ou la paludification), les forêts étudiées contenaient des stocks élevés de C au sein de l’horizon de matière organique, le sol minéral et le bois enterré. Les données ont aussi été utilisées pour évaluer le MBC-SFC3, un modèle national canadien du bilan du C, concernant son applicabilité aux pessières boréales humides de Labrador et d’ailleurs. Suite à l’ajustement de quelques paramètres, p.ex. des taux de décomposition, le MBC-SFC3 reproduisait bien le dynamisme mesuré des arbres vivants et du bois mort supraterrestre. Le MBC-SFC3 a initialement été développé pour les sites bien drainés et ne considère pas les processus associés avec les mousses ou l’humidité élevée du sol. Conséquemment, le MBC-SFC3 ne représentait pas les stocks élevés de C mesurés pour le bois enterré et pour le sol. Les modifications structurelles du MBC-SFC3 et d’autres modèles du C forestier sont nécessaires pour représenter adéquatement l’accumulation du C au sein de ces réservoirs. La précision des modèles du C forestier pourrait encore être améliorée par une différenciation des taux de décomposition selon le régime de perturbations, parce que la respiration du bois mort reflète les changements de la température et d’humidité associés avec une perturbation spécifique. Dans les pessières brûlés du Labrador, la respiration du bois mort était limitée par a faible humidité du bois et des températures élevées; dans les pessières vierges, par l’humidité élevée du bois et des températures basses. Dans les coupes à blanc, la végétation résiduelle empêchait le dessèchement du bois mort. Il s’y ensuivit que la respiration du bois mort y est nettement plus élevée en comparaison avec des pessières brûlés ou vierges. La décomposition du bois mort après coupe à blanc est aussi favorisée par la récupération plus rapide de la couche de mousses, diminuant conséquemment le dessèchement du bois mort par la conservation d’humidité, les transports vertical et horizontale d’eau et le refroidissement induit par l’humidité. Ainsi, les mousses sont les facteurs clés dans les cycles du bois mort et du C des pessières noires boréales au Labrador. L’auteur préconise la classification de ces pessières et des forêts semblables comme un groupe fonctionnel d’écosystèmes nommé : « pessières boréales humides » ; provisoirement définies comme « des écosystèmes forestiers avec une végétation terrestre dominée par les mousses et par conséquent associée avec des températures basses du sol, une humidité élevée, des taux de décomposition faibles et (en l’absence de perturbations) l’accumulation du bois enterré dans des couches organiques epaisses ». En outre, les mousses sont des éléments principaux des nombreuses forêts résineuses n’appartenant pas au biome boréal. Les processus régulés par les mousses tels l’enterrement du bois mort ou la paludification sont probablement importants pour le cycle global de C. La libération potentielle de grandes quantités de CO2 des réservoirs « bois enterré » et « sol » à la suite des changements climatiques exige une meilleure compréhension des transformations de la productivité des mousses et des limitations de la décomposition dues aux températures plus élevées et au taux d’humidités variables. Ainsi, les écosystèmes aux pertes potentielles de C élevées (p.ex. les pessières boréales humides) peuvent être identifiés et des mesures d’aménagement antagonistes peuvent être développées et implémentées. Traduction assistée par : Karl-Heinrich von Bothmer, Géry van der Kelen<br>Die vorliegende Arbeit untersucht die Einflüsse von Moosen auf den Totholz- und Kohlenstoff-(C)-Kreislauf in borealen Schwarzfichtenwäldern in Labrador, Kanada. Um den C-Kreislauf dieses humiden borealen Waldökosystems zu charakterisieren, wurden alle bedeutenden C-Speicher (lebende Bäume, stehendes und liegendes Totholz, organische Auflage, Mineralboden) von drei Primärwald-, neun Kahlschlags- und drei Brandflächen quantifiziert. Die C-Dynamiken der Bäume und des oberiridischen Totholzes der Untersuchungsflächen ähnelten denen von trockeneren und/oder wärmeren borealen Wäldern, während die organische Auflage, der Mineralboden und das begrabene Totholz bedingt durch von Moosen regulierte Prozesse wie Totholzeinlagerung und Paludifizierung besonders hohe C-Vorräte aufwiesen. Mit dem umfangreichen C-Datensatz wurde das CBM-CFS3, das nationale kanadische C-Modell, am Beispiel Labradors im Hinblick auf seine Anwendbarkeit in humiden borealen Wäldern evaluiert. Nach Anpassung ausgewählter Parameter, z.B. der Totholzabbauraten, wurden die gemessenen C-Dynamiken der Bäume und des oberiridischen Totholzes vom Modell abgebildet. Das CBM-CFS3 wurde ursprünglich für staunässefreie, terrestrische Waldstandorte entwickelt und berücksichtigt keine mit Moosen oder hoher Bodenfeuchte assoziierten Prozesse, so dass es die hohen C-Vorräte des begrabenen Totholzes und des Bodens nicht widerspiegelte. Eine adäquate Abbildung der Akkumulation von C in diesen Speichern erfordert strukturelle Änderungen des CBM-CFS3 und anderer Wald-C-Modelle. Die Genauigkeit von Wald-C-Modellen könnte darüber hinaus durch eine Differenzierung der Totholzabbauraten in Abhängigkeit vom Störungsregime verbessert werden, da störungsspezifische Veränderungen von Temperatur und Feuchte von der Totholzatmung widergespiegelt werden. Im Untersuchungsgebiet limitierten geringe Holzfeuchten und hohe Holztemperaturen die Totholzatmung auf Brandflächen. In Primärwäldern wirkten dagegen hohe Holzfeuchten und geringe Holztemperaturen hemmend. Auf Kahlschlägen verhinderte die verbleibende Vegetation die Austrockung des Totholzes, was zu signifikant erhöhten Atmungsraten im Vergleich zu Brand- und Primärwaldflächen führte. Zudem wird der Totholzabbau auf Kahlschlen durch eine schnellere Erholung der Moosdecke als auf Brandflächen gefördert, da Moose durch ihr hohes Wasserspeichervermögen, vertikalen und horizontalen Wassertransport und feuchte-induzierte Kühlung der Austrockung des Totholzes entgegenwirken. Moose sind somit ein Schlüsselfaktor im Totholz- und C-Kreislauf der humiden borealen Schwarzfichtenwälder Labradors. Die Autorin empfiehlt die Klassifikation dieser und ähnlicher borealer Wälder als eine funktionelle Ökosystemgruppe namens “humid boreal forests”; vorläufig definiert als “boreale Waldökosysteme mit durch Moose dominierter Bodenvegetation und damit assoziierten niedrigen Bodentemperaturen, hohen Bodenfeuchten, geringen Abbauraten und (in Abwesenheit großflächiger Störungen) der Akkumulation von begrabenem Totholz in mächtigen organischen Auflagen”. Auch außerhalb des borealen Bioms sind Moose ein wesentlicher Bestandteil vieler Nadelwälder. Durch Moose regulierte Prozesse wie Totholzeinlagerung und Paludifizierung sind daher wahrscheinlich relevant für den globalen C-Kreislauf. Die durch den Klimawandel bedingte potentielle Freisetzung von großen Mengen CO2 aus begrabenem Totholz und dem Boden macht ein besseres Verständnis der zu erwartenden Veränderungen von Mooswachstum und Abbauhemmnissen als Folge erhöhter Temperaturen und variabler Feuchteverhältnisse erforderlich. Somit können Ökosysteme mit potentiell hohen C-Verlusten, wie z.B. humide boreale Wälder, identifiziert und diesen entgegenwirkende Bewirtschaftungsmaßnahmen entwickelt und umgesetzt werden.
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Books on the topic "Bryophytes – Classification"

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Manyanga, Phelex. A checklist of Zimbabwean bryophytes. Southern African Botanical Diversity Network (SABONET), 2004.

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2008 Han'guk sŏnt'ae singmul mongnok: New list of bryophytes in Korea, 2008. Kungnip Sumogwŏn, 2008.

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author, Harpel Judith, Wagner, David H., 1945- author, and United States. Bureau of Land Management. Salem District, eds. Rare bryophytes of Oregon. U.S. Department of the Interior, Bureau of Land Management, Salem District, 2016.

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Sinikka, Piippo, ed. The bryophyte flora of Bromarv, Southwest Finland, based on Hans Buch's reliquiae and other collections. The Finnish Bryological Society, 2010.

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C, Srivastava S., ed. Indian hornworts: A taxonomic study. J. Cramer, 1991.

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1959-, He Si, ed. Zhongguo sheng wu wu zhong ming lu: Zhi wu : Plants / authors, Yu Jia, Si He. Ke xue chu ban she, 2013.

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Dr, Singh D. K., and Botanical Survey of India, eds. Hepaticae and anthocerotae of Great Himalayan National Park and its environs (HP), India. Botanical Survey of India, 2009.

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K, Singh S. Hepaticae and anthocerotae of great Himalayan national park and its environs (HP), India. Botanical Survey of India, 2009.

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9

K, Singh S. Hepaticae and anthocerotae of Great Himalayan National Park and its environs (HP), India. Botanical Survey of India, 2009.

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10

Liverworts and hornworts of southern Michigan. University of Michigan Herbarium, 1991.

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Book chapters on the topic "Bryophytes – Classification"

1

Ray, Samit, and Shewli Bhattacharya. "Classification of Bryophytes." In Manual for Bryophytes. CRC Press, 2021. http://dx.doi.org/10.1201/9781003208372-2.

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2

Buck, William R., and Bernard Goffinet. "Morphology and classification of mosses." In Bryophyte Biology. Cambridge University Press, 2000. http://dx.doi.org/10.1017/cbo9781139171304.004.

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3

Renzaglia, Karen S., and Kevin C. Vaughn. "Anatomy, development, and classification of hornworts." In Bryophyte Biology. Cambridge University Press, 2000. http://dx.doi.org/10.1017/cbo9781139171304.002.

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4

Crandall-Stotler, Barbara, and Raymond E. Stotler. "Morphology and classification of the Marchantiophyta." In Bryophyte Biology. Cambridge University Press, 2000. http://dx.doi.org/10.1017/cbo9781139171304.003.

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