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The phloroglucides of the ferns of the Dryopteris filix‐mas complex; i.e. D. abbreviata, D. filix‐mas s. str. and D. borreri (diploid and triploid) as well as those of D. villarii, subspvillarii and subsp. pallida were reinvestigated with improved semiquantitative analytical methods. The phloroglucides of D. aitoniana and D. athamantica were examined for the first time. The results (table 1) are compatible with the hypothesis, without proving it, that the allotetraploid species D. filix‐mas s. str. originated from a hybrid of D. abbreviata with D. villard (with subsequent doubling of its chromosomes) and the apogamous triploid D. remota from D. assimils with diploid D. borreri, and the equally apogamous triploid D. borreri from a hybrid of D. abbreviata (or a related diploid sexual taxon) with diploid D. borreri. D. aitoniana contains a large amount of trisflavaspidic acid but no filixic acid and differs in this respect from the three representatives of the D. filix‐mas complex.
The phloroglucides of the ferns of the Dryopteris filix‐mas complex; i.e. D. abbreviata, D. filix‐mas s. str. and D. borreri (diploid and triploid) as well as those of D. villarii, subspvillarii and subsp. pallida were reinvestigated with improved semiquantitative analytical methods. The phloroglucides of D. aitoniana and D. athamantica were examined for the first time. The results (table 1) are compatible with the hypothesis, without proving it, that the allotetraploid species D. filix‐mas s. str. originated from a hybrid of D. abbreviata with D. villard (with subsequent doubling of its chromosomes) and the apogamous triploid D. remota from D. assimils with diploid D. borreri, and the equally apogamous triploid D. borreri from a hybrid of D. abbreviata (or a related diploid sexual taxon) with diploid D. borreri. D. aitoniana contains a large amount of trisflavaspidic acid but no filixic acid and differs in this respect from the three representatives of the D. filix‐mas complex.
und Tadeus Reichsteind) (13. I. 75) Uneercm Freund, Herrn Prof. F. Santavf (Olornouc), zu seincm 60. Geburtstag (23.4. 1975) gewidmet. Summary. Thc phloroglucinols of Dvyopevis aemda from the Azores and from Brittany (France), D. aaorica and D. crispifolia, a new tctraploid specks endemic t o the Azores [a], have been investigatcd. Thc following two species recently analysed with insufficient amounts of material have bcen reinvestigatcd using improvcd methods: D. maderensis and 'D. dilatata' from Tenerife, a new species cndemic t o the Canary islands and described by Gibby et al. [s] as B.guanchim Gibby & Jemy.W c have now found that both these specks also contain much albaspidin, particularly the homologuc BA. Former results for these. and other species differing in somc details were corrected (sec Table 1) after careful reexamination of the old chromatograms.D . aemulu from all origins contains relatively large amounts of two new compounds: aemulin(1) and trisaemulin (20), thc structures of which werc provcd by degradation, NMR.-and massspectroscopy. Trisaemulin was present as a mixture of two hornologucs BBB and BAB. The latter is the first three-ring phloroglucinol found in nature which carries am acetyl group in the middle ring. so far only butyryl-groups were found in this position.D. azodca is diploid like D. madevsnsis and D. inkrmedia and a11 3 taxa contain practically the same range of phloroglucinols. These facts are in agreement with conclusions based on morphology and cytology, which suggest that thew three taxa arc essentially cbnspecific. ).-_.._
Josef v. Euw4) und Tadeus Reichstein4) (13. IV. 76) 'The phloroglucinols of two fern hybrids from England and Scotland, of authentic 'Aspidium remotum' A. BRAWN and of Dryopteris aemula (AITON) 0. KUNTZE from Ireland'. -Summary. The phloroglucinols of Dryopteris aemula (AITON) 0. KUNTZE from Ireland, of two Dryopteris hybrids from England (D. x brathaica FRASER-JENKINS et REICHST. (in preparation) and D. x pseudo-abbreviata JERMY) and of a sample of A. BRAUN'S original collection of 'Aspidium remotum' (= D. remota (A. BR.) DRKJCE) have been analysed. D . aemula from Ireland gave the same results as plants recently obtained from the Azores, England, Madeira and northern France. D. x brathaica, a tetraploid hybrid found only once (1854) in England (Windcrmere), but still surviving in cultivation (in Oxford Botanic Garden), has long been confused with triploid apogamous D. remota, and until recently there has been some uncertainty as to which of the two plants the name D . remota (-4. BR.) DRUCE should correctly be applied to. For morphological, geographical and cytological reasons it has been assumed that D . x brathaica could be the hybrid of D. carthusiana (VILL.) H. P. F u c~s x D. falix-mas (L.) SCHOTT. The chemical results are in accordance with this assumption. Also the phloroglucinols of D. x brathaica are different from those of the triploid D. remota. It is therefore possible to differentiate between old herbarium specimens of these two morphologically very similar plants by means of chemical methods, even when no fresh material is available for spore examination or cytological investigation. Chemical analysis of a piece of A. BRAUN'S original collection of 'Aspidium remotum'(deposited in Berlin) clearly showed that it contained exactly the same phloroglucinols as the triploid taxon. We consider this to be additional and final proof that the name D. remota is correctly attributed t o the triploid apogamous taxon.D . pseudo-abbreviata was assumed to be a hybrid of D . aemula x D . oreades Fomin (= D . abbreviata (DC.) NEWM.). Our chemical results strongly support the hypothesis that D . aemula is indeed one parent; they are less unequivocal for the second as they would fit not only for D . oreades but equally for D. pseudo-mas (WOLLASTON) HOLUB et POUZAR (= D . borreri NEWM.). Spore morphology is more compatible with the latter.Improved methods are given for separating natural phloroglucinols on TLC. This allowed corrections of former rcsults and led to the detection that the compound present in D . innequalis [4r] and D . sacrosancta [4w] assumed to be trisaspidinol (8 in [4r]) in reality was trispara-aspidin (14 in [4e]). This was confirmed by its NMR. spectrum and reductive cleavage.
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