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220 results for “Glutinosae”

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zenodo32/100

Fig. 1 in Diterpenoids caryopterisoids D - Q and iridoid glucoside derivatives caryopterisides F - H from Caryopteris glutinosa

Fig. 1. Chemical structures of caryopterisoids D - Q (1 – 14) and caryopterisides F H (15 - 17) from Caryopteris glutinosa.

opennotspecifiedDec 2020View details →

zenodo32/100

Fig. 4 in Diterpenoids caryopterisoids D - Q and iridoid glucoside derivatives caryopterisides F - H from Caryopteris glutinosa

Fig. 4. Cell-based estrogen biosynthesis assays for the isolated compounds (A), WB of caryopterisoid K (8) (B) and its quantitative results (C), qRT-PCR (D), and molecular docking (E). DMSO, control; FSK, 10 μM forskolin, positive control for the increase of estrogen E2; LET, 10 nM letrozole, positive control for the decrease of estrogen E2; CREB, cAMP-response element binding protein, a key protein in the upstream of the signaling pathway of estrogen biosynthesis; pCREB, phosphorylated CREB; Form, 50 μM formestane, positive control for the expression of aromatase; GAPDH, glyceraldehyde-3-phosphate dehydrogenase, reference gene; KI, inhibition constant. *, p <0.05; **, p <0.01; ***, p <0.001; compared with the control (n = 3).

opennotspecifiedDec 2020View details →

dryad32/100

Data from: High genetic diversity and distinctiveness of rear-edge climate relicts maintained by ancient tetraploidisation for Alnus glutinosa

Open the record for dataset details and reuse information.

publicOct 2013View details →

dryad28/100

Data from: De novo discovery and multiplexed amplification of microsatellite markers for black alder (Alnus glutinosa) and related species using SSR-enriched shotgun pyrosequencing.

Recent developments in sequencing technologies and bioinformatics analyses provide an unprecedented opportunity for cost and time effective high quality microsatellite marker discovery in non-model organisms for which no genomic information is available. Here, we use shotgun pyrosequencing of a microsatellite-enriched library to develop, for the first time, microsatellite markers for Alnus glutinosa, a keystone tree species of European riparian woodland communities. From a total of 17,855 short sequences, we identified 590 perfect microsatellites from which 392 had designed primers. A subset of 48 loci were tested for amplification, twelve of which were polymorphic in A. glutinosa. These twelve loci were successfully co-amplified in a single multiplex PCR experiment and validated for population genetics applications. In addition, ten and eight of these microsatellites were found to be transferable to the related A. incana and A. cordata species. The developed multiplex of 12 microsatellite markers therefore provides new opportunities for experimental evolutionary and forest genetics research in Alnus.

opencc-zeroDec 2010View details →

dryad28/100

Data from: Higher genetic diversity in recolonized areas than in refugia of Alnus glutinosa triggered by continent-wide lineage admixture

Genetic admixture is supposed to be an important trigger of species expansions because it can create the potential for selection of genotypes suitable for new climatic conditions. Up until now, however, no continent-wide population genetic study has performed a detailed reconstruction of admixture events during natural species expansions. To fill this gap, we analysed the postglacial history of Alnus glutinosa, a keystone species of European swamp habitats, across its entire distribution range using two molecular markers, cpDNA and nuclear microsatellites. CpDNA revealed multiple southern refugia located in the Iberian, Apennine, Balkan and Anatolian Peninsulas, Corsica and North Africa. Analysis of microsatellites variation revealed three main directions of postglacial expansion: (i) from the northern part of the Iberian Peninsula to Western and Central Europe and subsequently to the British Isles, (ii) from the Apennine Peninsula to the Alps and (iii) from the eastern part of the Balkan Peninsula to the Carpathians followed by expansion towards the Northern European plains. This challenges the classical paradigm that most European populations originated from refugial areas in the Carpathians. It has been shown that colonizing lineages have met several times and formed secondary contact zones with unexpectedly high population genetic diversity in Central Europe and Scandinavia. On the contrary, limited genetic admixture in southern refugial areas of A. glutinosa renders rear-edge populations in the Mediterranean region more vulnerable to extinction due to climate change.

opencc-zeroDec 2014View details →

zenodo28/100

Text-fig. 9. a–e: Carya aff. minor. a: Terminal leaflet, Oriolo MSF 755. b: Oriolo MSF 755. c: Oriolo MSF 766. d: Oriolo MSF 768. e: Oriolo MSF 635. f, g: Pterocarya aff. fraxinifolia. f: Fruit, Oriolo MSF 632. g: Leaflet, Oriolo MSF 632a. h–j: Alnus aff. glutinosa subsp. barbata. h: Oriolo MSF 852. i: Oriolo MSF 850. j: Seed cone, Oriolo MSF 987. k–o: Corylus aff. avellana. k: Leaf, Oriolo MSF 841. l: Fruit, Oriolo MSF 1001. m: Fruit, Oriolo MSF 1022. n: Fruit, Oriolo MSF 1003. o: Fruit, Oriolo MSF 1022. Scale bars 50 mm (a–e, g–i), 10 mm (f, j–o). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome

Text-fig. 9. a–e: Carya aff. minor. a: Terminal leaflet, Oriolo MSF 755. b: Oriolo MSF 755. c: Oriolo MSF 766. d: Oriolo MSF 768. e: Oriolo MSF 635. f, g: Pterocarya aff. fraxinifolia. f: Fruit, Oriolo MSF 632. g: Leaflet, Oriolo MSF 632a. h–j: Alnus aff. glutinosa subsp. barbata. h: Oriolo MSF 852. i: Oriolo MSF 850. j: Seed cone, Oriolo MSF 987. k–o: Corylus aff. avellana. k: Leaf, Oriolo MSF 841. l: Fruit, Oriolo MSF 1001. m: Fruit, Oriolo MSF 1022. n: Fruit, Oriolo MSF 1003. o: Fruit, Oriolo MSF 1022. Scale bars 50 mm (a–e, g–i), 10 mm (f, j–o).

opencc-by-4.0Aug 2022View details →

zenodo28/100