Terpenoids and bibenzyls from some New Zealand liverworts

Four liverworts, Marchantia berteroana, M. foliacea, Plagiochila stephensoniana and Porella elegantula collected in New Zealand were chemically investigated. M. berteroana contains cuparene and (?)-2-hydroxycuparene as the major components. γ-Cadinene is the major component of M. foliacea. 4-Hydroxy-3′-methoxybibenzyl is a chemical marker for P. stephensoniana which belongs to the non-pungent type of Plagiochila species. P. elegantula synthesizes perrottetianal and belongs to the non-pungent type of Porella species.     

Cuparane- and isocuparane-type sesquiterpenoids in liverworts of the genus Herbertus

Canadian and Japanese Herbertus aduncus, Japanese H. sakuraii and Colombian H. subdentatus belonging to the Jungermanniales (Hepaticae) were chemically investigated. The previously known entcuparane- and novel isocuparane-type sesquiterpenoids are the major components which are of importance as chemical markers in the Herbertaceae.     

Lunularic acid and related compounds in liverworts,algae and Hydrangea

Lunularic acid and lunularin were detected in 76 species of hepatics, but not in any of the Anthrocerotales or Algae examined. Lunularic acid, lunularin, 3,4′-dihydroxystilbene and a glycoside of lunularic acid were also identified in extracts of Hydrangea macrophylla roots, together with hydrangenol, hydrangeic acid and their glucosides.     

Flavonoids of the liverwort Marchantia polymorpha

The major flavonoids of Marchantia polymorpha var. polymorpha and aquatica are the 7-O-β-d-glucuronides of apigenin and luteolin, luteolin 3′-O-β-d-glucuronide, luteolin 7,3′-di-O-β-d-glucuronide, and the 7,4′-di-O-β-d-glucuronides of apigenin and luteolin. These are accompanied by minor amounts of apigenin, luteolin, luteolin 3′,4′-di-O-β-d-glucuronide and luteolin 7,3′,4′-tri-O-β-d-glucuronide. All the luteolin di- and triglucuronides except the 3′,4′-di- substituted compound are new natural products.     

Urease and urea amidolyase: Determination of activity in liverworts

Using highly sensitive techniques, we have investigated urea degradation in the liverworts and found that they have high urease but no detectable urea amidolyase activity.     

Evidence of biosynthetic simplicity in the flavonoid chemistry of the ricciaceae

The major flavonoids in Riccia crystallina are naringenin and its 7-O-glucoside, apigenin 7-O-glucoside and apigenin 7-O-glucuronide and derivatives. Ricciocarpus natans is a rich source of luteolin 7,3′-di-O-glucuronide and also contains the 7-O-glucuronides of apigenin and luteolin and the 3′-O-glucuronide of luteolin. A parallel between the production of biosynthetically simple flavonoids and reduced morphology is evident among these liverworts.     

Sesquiterpenes from Japanese liverworts

Five Japanese liverworts (Bazzania sp.) were examined for sesquiterpenes. B. japonica and B. pompeana contained two new drimane-type sesquiterpene esters, albicanyl 3,4-dihydroxycinnamate and albicanyl 2,4dihydroxycinnamate. Tridensenone, a new aromadendrane-type sesquiterpene ketone was isolated from B. tridens. The stereostructures of these new sesquiterpenes were elucidated mainly by spectrometry. Barbatane-, bazzanane- and cuparane-type sesquiterpenes were found in all of the five species investigated. These sesquiterpenes, along with the new drimane- and aromadendrane-type sesquiterpenes are useful chemosystematic markers.     

Prelunularic acid in liverworts

Prelunularic acid, the first example of an intermediate with a ‘pre-aromatic’ structure in the phenylpropanoid-polymalonate pathway, was isolated from suspension-cultured cells of Marchantia polymorpha. Its structure, including its absolute configuration, was assigned on the basis of spectral properties, direct conversion into lunularic acid, and CD measurements on the bis(p-dimethylaminobenzoate) of the methyl ester. Prelunularic acid was also detected in several liverworts of Marchantiales and Jungermanniales, and appears to be the immediate precursor of lunularic acid instead of the previously postulated hydrangenol or hydrangeic acid.     

Sesquiterpenes of six Porella species (hepaticae)

The distribution in six Porella species of drimane-, aromadendrane- and pinguisane-type sesquiterpenes and norsesquiterpenes is described. The sharp pungent substance of P. gracillissima, P. fauriei and P. macroloba is (+)-tadeonal.     

On the occurrence of lignin or polyphenols in some mosses and liverworts

Six species of mosses (Musci) and two species of liverworts (Hepaticae) have been investigated for the presence of lignin by oxidative degradation. The results clearly demonstrate that these species are devoid of ligrin, but contain other types of phenolic cell wall material.     

Sesquiterpenoids of Riccardia and Pallavicinia species

Riccardia species (Metzgeriales) contain various types of sesquiterpenes. R. jackii produces ent-selinane-, ent-aromadendrane-and ent-bicyclogermacrane-type sesquiterpenes together with (R)-cuparene and α-barbatene. Aneura pinguis (= Riccardia pinguis) is chemically quite different from R. multifida and R. jackii. The former produces a large amount of pinguisone. R. multifida contains 6-(3-methyl-2-butenyl)-indole and (+)-β-elemene as the major components. Pallavicinia longispina (Dilaenaceae; Metzgeriales) produces mainly spathulenol. The chiral properties of the sesquiterpenes isolated from R. jackii are quite similar to those of red algae, Laurencia species.     

Auxin metabolism in mosses and liverworts

The plant hormone auxin (indole-3-acetic acid, IAA) is involved in the control of many phenomena during plant development. By characterizing steady-state free and conjugated IAA levels using a stable isotope dilution method coupled with gas chromatography- selected ion monitoring- mass spectrometry, this paper provides a detailed characterization of IAA metabolism in five liverworts, four mosses, and two tracheophytes. Long-term IAA conjugation patterns were monitored by incubating actively growing tissue with (14)C-IAA and then analyzing the de novo synthesis of IAA conjugates with radioimaging techniques. The liverworts, mosses, and tracheophytes can be differentiated by the total amount of IAA metabolites, the proportion of free and conjugated IAA, the chemical nature of their IAA conjugates, and the rates of IAA conjugation. Our tentative conclusion is that the liverworts appear to employ a biosynthesis-degradation strategy for the regulation of free IAA levels, in contrast to the conjugation-hydrolysis strategy apparently used by the mosses and tracheophytes. Such alternative metabolic strategies may have profound implications for macroevolutionary processes in these plant groups.     

The concentrations of lunularic acid and prelunularic acid in liverworts

The amounts of lunularic acid in suspension cultured cells of Marchantia polymorpha and thallus of Conocephalum conicum were carefully re-exami     

Sesquiterpenes of thalloid liverworts of the genera Conocephalum,Lunularia, Metzgeria and Riccardia

Thalloid liverworts of orders Metzgeriales and Marchantiales elaborate essential oils distinguishable from those of the Jungermanniales by the absence of β-barbatene and anastreptene. Riccardia sinuata elaborates a novel tricyclic exomethylene sesquiterpene of as yet undetermined structure. Conocephalum conicum elaborates cadinene-type sesquiterpenes. β-Cadinene from the latter species is clearly enantiomeric to the same product from vascular plants.     

Pungent sesquiterpene lactones of the european liverworts Chiloscyphus polyanthus and Diplophyllum albicans

The characteristic pungency of the European liverwort, Chiloscyphus polyanthus, is due to a mixture of four sesquiterpene lactones, two new structures ent-5β-hydroxydiplophyllin and ent-3-oxodiplophyllin, and the previously known diplophyllin and diplophyllolide. A new dihydrodiplophyllin, together with the pungent diplophyllolide and diplophyllin, has been isolated from Diplophyllum albicans. Ent-dihydrodiplophyllolides derived from the above pungent diplophyllolides produce intense numbness of the tongue. All pungent sesquiterpene lactones showed inhibitory activity towards the germination and root elongation of rice husks.     

Free sterols of the red alga Gigartina skottsbergii

The free sterols of the red alga Gigartina skottsbergii have been identified by means of GC and GC/MS analyses. The mixture contained saturated and unsaturated C²⁷, C²⁸ and C²⁹ sterols. The major component was cholest-5-en-3β-ol. Cholesta-5,24-dien-3β-ol (desmosterol) was present in low proportion but no side chain hydroxylated components were detected.     

浙江百山祖自然保护区叶附生苔资源

本文对百山祖自然保护区的叶附生苔资源及其环境作了简要论述。业已发现,百山祖有叶附生苔5科13属38种,是我国亚热带地区叶附生苔的分布中心之一,特别是十九源和百山祖冷杉附近,海拔较高、空气湿度大,是叶附生苔生长的良好环境。     

Sesquiterpenes of Barbilophozia species

Two isomeric olefins, α- and β-barbatene, apparently of a new tricyclic sesquiterpene skeleton (that of gymnomitrol), have been found in the liverworts Barbilophozia barbata, B. floerkei, B. lycopodioides, and B. attenuata. Additional components identified are alkanes, calamenene and α-alaskene. GLC suggests the presence of caryophyllene, longifolene, bazzanene and α-cedrene in minor amounts.