Aporphine alkaloids and lignans in heartwood of Liriodendron tulipifera

The following compounds were isolated from heartwood of Liriodendron tulipifera: glaucine, dehydroglaucine, asimilobine, N-acetylnornuciferine, norushinsunine, liriodenine, O-methylatheroline, (+)-syringaresinol, (+)-syringaresinol dimethyl ether and syringaldehyde. The occurrence of 1-benzyltetrahydroisoquinoline alkaloids also has been indicated by mass spectroscopy. Some characteristic spectral properties of these aporphine alkaloids and their probable biosynthetic pathways are discussed.     

Lignans and aporphine alkaloids in bark of Liriodendron tulipifera

Lirionol, a novel tetracyclic lignan, has been isolated from the bark of Liriodendron tulipifera and its structure determined by spectroscopic analysis. In addition, syringic acid methyl ester, (+)-pinoresinol, (+)-syringaresinol, N-(2-hydroxy-2-phenylethyl)benzamide and O-methyl-N-norlirinine have also been isolated. The structures of lirinine and related compounds isolated from the leaves of this tree-species by Yunusov et al. are also discussed.     

Formation and vertical distribution of sapwood and heartwood in Cryptomeria japonica D. Don

The formation and vertical distribution of sapwood and heartwood were studied with a 45-year-old Cryptomeria japonica D. Don. The tree was grown at a plantation with 1.5 m × 3.0 m spacing near Miao-Li, Taiwan and was felled on 27 February 1992. The thickness of sapwood and heartwood was expressed by a ring count and a linear measurement. The east-west (E-W) wood strips were collected from 0.3 m above ground upwards to the top of the tree at 2.5 m intervals. The sapwood thicknesses from the base to the 10.3 m tree level height are around 20–22 growth rings and 42±2 mm. At the top of the tree, the sapwood thickness is narrower. The heartwood, which decreases in thickness with increasing tree level heights is not found at the top of the tree. The heartwood appears as a conical shape in the tree trunk. There is no statistical difference in sapwood/heartwood thickness between E-W aspects. Tree level heights and the tree level age were found to be important parameters in determining the thickness of sapwood/heartwood.     

Liriodendronine,an oxoaporphine pigment from discolored sapwood of Liriodendron tulipifera

A new violet oxoaporphine alkaloid. liriodendronine, has been isolated from the discolored sapwood of Liniodendron tulipifera and its structure determined by spectroscopic methods and by conversion into a corunnine-type compound, 2-O,N-dimethylliriodendronine. UV studies demonstrated that the compound exists primarily as a quinone-methide in a neutral medium, a dianion in base, an isoquinolinium ion in weak acid, and as an antiaromatic conjugate acid in conc H₂SO₄.     

Size- and Age-dependent Variation in the Properties of Sap- and Heartwood in Black Locust (Robinia pseudoacaciaL.)

Dissection and mechanical bending experiments showed that the cross-sectional area and elastic moduli of sap- and heartwood varied within the trunk and branches as a function of the distance from the top of a 43-year-old black locust tree (Robinia pseudoacaciaL.). Wood in branches less than 1 m from the top of the tree consisted entirely of sapwood; the majority of the wood from more basipetal (and older) parts of the tree was heartwood. The Young's elastic moduli of sap- and heartwood increased towards the base of the trunk, and, on average, the modulus of the sapwood was 35%less than that of the heartwood. Younger, more distal tree limbs, therefore, were more flexible than older portions of the same tree. Simple bending experiments showed that the flexural rigidity of young limbs was governed by the location, physical properties, and the relative quantities of the two types of wood. The rigidity of limbs increased toward the base of the tree, and was dominated by sapwood in young limbs and by heartwood in the oldest parts of the tree. These trends predict that the younger, distal limbs of this tree can more easily deflect and bend in the wind, thereby reducing drag and the total bending moment on the tree trunk, while older limbs and the trunk are sufficiently rigid to support static self-loadings. Further study, however, is required to determine whether the trends reported here apply to all trees of this species and to trees of different species.     

Four new N-acetylnoraporphine alkaloids from Liriodendron tulipifera

Four new naturally occurring N-acetylnoraporphine alkaloids were obtained from the heartwood of Liriodendron tulipifera; (?)-N-acetylanonaine, (?)-N-acetylnornuciferine, (?)-N-acetylasimilobine, and (?)-tuliferoline. Structure determination was accomplished by physical and chemical methods.     

Natural wood colouring process in Juglans sp. (J. nigra, J. regia and hybrid J. nigra 23 ×J. regia) depends on native phenolic compounds accumulated in the transition zone between sapwood and heartwood

 Radial distribution of soluble phenolics was investigated at different heights in stems of Juglans nigra, J. regia and hybrids J. nigra 23 × J. regia. Four major phenolic compounds were studied: hydrojuglone glucoside (HJG), quercitrin (QUER) and two unknown compounds characterized as two ellagic acid derivatives E1 and E2. HJG and E1 content increased gradually in the sapwood, peaked in the sapwood-heartwood transition zone, and decreased drastically in the heartwood. QUER was accumulated preferentially around the transition zone, and its content was relatively low in the outer part of the sapwood and in the inner part of the heartwood. E2 content was low in the sapwood and increased in the heartwood. The heartwood formation was marked by the accumulation of new soluble compounds. The relationship between wood extractives and wood colour were evaluated and discussed. HJG was considered to be a major precursor of heartwood colour providing chromophores through hydrolysis (deglucosylation), oxidation and polymerization processes. Received: 2 September 1997 / Accepted: 23 November 1997     

Additional alkaloids from Laurelia philippiana and L. novae-zelandiae

Asimilobine, anonaine, noreorydine, nornantenine, (+)-reticuline and the new alkaloid, 4-hydroxyanonaine, were isolated from Laurelia philippiana bark. The biogenetically related obovanine, oxoputerine and (?)-romneine, not known as a natural product, were obtained from the bark of L. novae-zelandiae. The occurrence of (R)-norlaudanosoline-derived alkaloids in L. novae-zelandiae is a distinctive feature of this tree. Neither L. novae-zelandiae nor L. philippiana accumulate dimeric benzylisoquinoline alkaloids to any appreciable extent in the trunk bark, differing in this respect from L. sempervirens, the only other Laurelia species.     

Relationship of heartwood traits with diameter growth, implications for genetic selection in Pinus radiata

The heartwood of radiata pine (Pinus radiata D. Don) is not favoured commercially because of its darker appearance, unreliable durability and difficulty to treat chemically; consequently, light-coloured sapwood, which is more easily treated with decay-resistant chemicals, is of more value. To decrease the amount of heartwood or increase sapwood cross-sectional area by genetic selection, the genetics of sapwood cross-sectional area (SWA), sapwood area percentage (SWAP) and number of heartwood rings (HWR) is of interest. We investigated genetic variation in these three variables from increment cores from trees from two trial series, each planted at two sites, from a total of some 330 families (189 were half-sib and 142 were full-sib) with 10 to 30 individuals assessed per family. Trials were assessed between 16 and 23 years old when all trees had started to develop heartwood. The three sapwood-related traits were moderately heritable across pairs of sites ( h ^ i 2 $ {\widehat{h}}_i^2 $ = 0.2 to 0.4) indicating opportunity for selection. SWA was strongly correlated (r _a ?=?0.9) with diameter. SWAP and HWR were also strongly correlated (r _a ?=??0.9). The number of HWR was independent of tree diameter, providing the opportunity through genetic selection to reduce heartwood area whilst increasing tree growth rate.     

Heartwood and sapwood development within maritime pine (<Emphasis Type="Italic">Pinus pinaster </Emphasis>Ait.) stems

Heartwood and sapwood development in maritime pine (Pinus pinaster Ait.) is reported based on 35 trees randomly sampled in four sites in Portugal. It was possible to model the number of heartwood rings with cambial age. The heartwood initiation age was estimated to be 13 years and the rate of sapwood transformation into heartwood was 0.5 and 0.7 rings year^–1 for ages below and above 55 years, respectively. Reconstruction of heartwood volume inside the tree stem was made by visual identification by image analysis in longitudinal boards along the sawn surfaces. This volume was integrated into the 3D models of logs and stems developed for this species representing the external shape and internal knots. Heartwood either follows the stem profile or shows a maximum value at 3.8 m in height, on average, while sapwood width is greater at the stem base and after 3 m remains almost constant up the stem. Up to 50% of tree height heartwood represents 17% of stem volume, in 83-year-old trees and 12–13% in 42 to 55-year-old trees. Tree variables such as stem diameter, DBH and tree total height were found to correlate significantly with the heartwood content.     

Respiration in the sapwood and heartwood of Robinia pseudoacacia

The respiratory activity of distinct sapwood and heartwood annual rings of the stem of Robinia pseudoacacia L. has been investigated. The oxygen uptake and the carbon dioxide release in the inner parts of the sapwood is enhanced in comparison with that in the outer parts. The heartwood rings have no measureable gas exchange.     

Alkaloids of Thermopsis Lupinoides

Ammodendrine, together with seven other known lupin alkaloids, was isolated from Thermopsis lupinoides. (+)-Lupanine (+)-17-oxolupanine occurred together with (?)anagyrine, (?)-baptifoline, (?)-cytisine, (?)-N-methylcytisine (?)N-formylcytisine. These alkaloids have the opposite stereochemistry to that of (+)-lupanine and (+)-17-oxolupanine. The distribution of alkaloids in fresh flowers, leaves, stems roots of this plant was also examined.     

Fumariaceae alkaloids including the biogenetic precursor of cularine

Corydalis claviculata has yielded (+)-crassifoline, the first 7,8,3′,4′-oxygenated benzylisoquinoline and biogenetic precursor of cularine, as well as the new cularine alkaloids (+)-sarcocapnidine, (+)-claviculine and (+)-O-methylcularicine.     

A statistical model for the prediction of the number of sapwood rings in Scots pine (Pinus sylvestris L.)

Dendrochronology is a well-established dating method for wooden objects, but due to surface processing of construction timber or natural degradation the dating of historical wood often relies on a prediction of the number of missing rings based on sapwood statistics. Since Scots pine (Pinus sylvestris L.) is one of the most common tree species in north-western Europe, the absence of reliable sapwood statistics and models for the prediction of missing sapwood rings for pine samples is remarkable. We have therefore produced sapwood statistics based on data from 776 pine trees with ages from 15 to 345 years. The material consists of both living trees and historical timber, with varying growth rates, geographic settings, and from different soil types. When the whole material is considered, the average age of the trees is 103 years, and the number of sapwood rings is 54 ± 15 (1 SD), but range from 18 to 129. Trees less than 100-years in age contained 46 ± 11 (1 SD) sapwood rings and had an average tree-ring width (TRW) of 1.76 mm. With increasing age, the average TRW decreased while the number of sapwood rings increased. The average TRW of 101–200-year-old trees is 0.99 mm while the samples contained 63 ± 12 (1 SD) sapwood rings. For trees older than 201 years, the average TRW is 0.64 mm while the number of sapwood rings increased to 85 ± 16 (1 SD). The two most important factors in determining the number of sapwood rings for a given tree when only heartwood statistics are available proved to be (i) the number of heartwood rings and (ii) the average TRW of the heartwood rings. For incomplete samples, we have therefore developed a statistical model based on the sample’s heartwood rings (number and average width) to compute a prediction interval for the total number of rings. The sapwood and heartwood statistics suggest a statistical model for the number of sapwood rings with mean that increase with the number of heartwood rings. Furthermore, the average number of sapwood rings decreases with the mean width of the heartwood rings. However, the predictive power of the mean width is limited when the number of heartwood rings has already been taken into account. Thus, we suggest making predictions for the number of sapwood rings using only the number of heartwood rings. Predictions of the number of sapwood rings based on the statistical model where convincing in the case of the three different datasets that were analysed. The certainty in these predictions was such that the width of the 80% and 95% prediction intervals ranged 28–34 and 45–52 sapwood rings, respectively. Additionally, we demonstrate how make predictions when there is information about the number of remaining sapwood rings in a given sample. To make the sapwood model available, we present a free online R package for fitting our models and an online software dashboard.     

Sapwood characteristics of Quercus robur species from the south-western part of the Pannonian Basin

We analysed sapwood characteristics in 344 pedunculate oak (Quercus robur L.) samples from the south-western part of the Pannonian Basin. The samples came from 13 sites, located in Slovenia, Croatia and Serbia. The trees had an average of 13.3 sapwood rings, with a minimum of 5 and maximum of 32. Fifteen log-log linear regression models were employed to assess the statistical relationship between sapwood and heartwood variables. The number of sapwood rings (N_SW), which is usually needed in dendroarchaeological dating, is significantly related to the number of heartwood rings (N_HW), heartwood width (W_HW) and heartwood growth rate (G_HW). Older and more slowly growing trees had a higher average number of sapwood rings. Using N_HW and W_HW, we employed an additional multiple regression model and calculated coefficients for N_SW predictions for real-world dendroarchaeological dating from the south-western part of the Pannonian Basin.     

Soluble carbohydrates of Pinus sylvestris L. sapwood and heartwood

Summary The amounts of glucose, fructose, sucrose, arabinose/galactose, raffinose/stachyose and starch were investigated in the outer sapwood, innermost sapwood, transition zone and heartwood of four stems of Pinus sylvestris L. The samples were taken in October and the determination of the compounds was done enzymatically. It was not possible to distinguish arabinose from galactose and raffinose from stachyose. The amounts of glucose, fructose and sucrose were greatest in the outer sapwood and decreased gradually towards the innermost sapwood and the heartwood. In the outermost heartwood glucose, fructose and sucrose were only present in trace amounts. Raffinose/stachyose showed highest concentrations in the outer sapwood and decreased towards the heartwood. In contrast, the concentrations of arabinose/galactose increased towards the heartwood and the greatest amount was found in the inner heartwood. When identified by thin-layer chromatography (TLC), arabinose was found to be present in greater amounts than galactose. The amount of starch decreased markedly towards heartwood. However, the amounts of sugars in all the studied stems was very variable. The changes in the amounts of carbohydrates in the different zones of the stems and the possible relationships of these phenomena with heartwood formation are discussed.     

Spatial Patterns in Hyphal Growth and Substrate Exploitation within Norway Spruce Stems Colonized by the Pathogenic White-Rot Fungus Heterobasidion parviporum

In Norway spruce, a fungistatic reaction zone with a high pH and enrichment of phenolics is formed in the sapwood facing heartwood colonized by the white-rot fungus Heterobasidion parviporum. Fungal penetration of the reaction zone eventually results in expansion of this xylem defense. To obtain information about mechanisms operating upon heartwood and reaction zone colonization by the pathogen, hyphal growth and wood degradation were investigated using real-time PCR, microscopy, and comparative wood density analysis of naturally colonized trees with extensive stem decay. The hyphae associated with delignified wood at stump level were devoid of any extracellular matrix, whereas incipient decay at the top of decay columns was characterized by a carbohydrate-rich hyphal sheath attaching hyphae to tracheid walls. The amount of pathogen DNA peaked in aniline wood, a narrow darkened tissue at the colony border apparently representing a compromised region of the reaction zone. Vigorous production of pathogen conidiophores occurred in this region. Colonization of aniline wood was characterized by hyphal growth within polyphenolic lumen deposits in tracheids and rays, and the hyphae were fully encased in a carbohydrate-rich extracellular matrix. Together, these data indicate that the interaction of the fungus with the reaction zone involves a local concentration of fungal biomass that forms an efficient translocation channel for nutrients. Finally, the enhanced production of the hyphal sheath may be instrumental in lateral expansion of the decay column beyond the reaction zone boundary.To grow to great heights, trees continually replace their water- and nutrient-conducting elements. Older elements, such as the heartwood that is formed in many trees, gradually become nonconductive. In contrast to the living sapwood, heartwood lacks active defense mechanisms against microbes. However, lignin, the polymer coating cell wall polysaccharides, is highly resistant to microbial degradation. In fact, white-rot fungi, besides having evolved the ability to tolerate or detoxify the secondary metabolites accumulating in heartwood, are the only organisms capable of efficiently degrading lignin. Following establishment in the heartwood of living trees, the colonies of pathogenic white-rot fungi expand and eventually also threaten the conductive sapwood.The white-rot fungus Heterobasidion annosum sensu lato, composed of three species with overlapping geographic distributions and host ranges in Europe (23), is the most important pathogen of Norway spruce (Picea abies L. Karst) in boreal forests. Primary infection of Norway spruce stands by H. annosum sensu lato takes place through fresh thinning stumps or wounds on roots and at the base of the stem. Basidiospores landing on these entrance points give rise to mycelia which colonize the root systems, and eventually the fungus spreads into the stem heartwood. At sites infested with Heterobasidion parviporum, a species primarily restricted to Norway spruce, roots of saplings can become infected by the fungus after around 10 years of growth (25). Stem colonization usually initiates only after the heartwood has started to develop, which in Norway spruce takes place in trees 25 to 40 years old (17). Due to relatively rapid axial spread within heartwood, the decay column caused by H. annosum sensu lato often is up to 10 m high in the stems of mature Norway spruce trees.In response to sapwood challenge by an expanding heartwood-based colony of H. annosum sensu lato, Norway spruce forms a so-called reaction zone (RZ) in the border area between healthy sapwood and colonized heartwood. This xylem defense is characterized by high pH due to increased carbonate content and enrichment of phenolic compounds, particularly lignans, some of which have shown antifungal properties in bioassays (14, 30, 31). Although several wood decay fungi are able to eventually penetrate the RZ regions formed in trees, the strategies employed by fungi to breach these unique defense barriers are poorly understood (24). The purpose of this study was to obtain information about the mechanisms operating in heartwood colonization and expansion of the decay column via penetration of the RZ. To do this, we examined spatial growth of H. parviporum and the associated substrate exploitation patterns within naturally colonized mature stems of Norway spruce.     

Formation of heartwood substances in the stem of Robinia pseudoacacia L.

Summary The activities of two key enzymes in flavonoid biosynthesis, phenylalanine ammonia-lyase (PAL, E.C. 4.3.1.5) and chalcone synthase (CHS, E.C. 2.3.1.74) were determined in the trunkwood of Robinia pseudoacacia L. The trees under investigation were cut at different times of the year (September, November, January and April). At all times PAL is active, both in the youngest wood layer (the outermost growth ring) and at the sapwood heartwood boundary. On the other hand, CHS is active exclusively in the vicinity of the heartwood boundary. The results indicate that PAL is involved both in the formation of lignin (outermost annual ring), and in flavonoid biosynthesis (heartwood boundary). Highest activity of both PAL and CHS could be measured at the sapwood heartwood boundary in the tree felled in November, indicating that heartwood formation was occurring mainly at that time. The flavonoids accumulated in the heartwood are obviously formed in situ and seem to be transported only to a minor extent — if at all — via the phloem and the ray cells to the heartwood.     

Source of some minor alkaloids in Glaucium flavum

Air oxidation of glaucine leads to 7,6′-dehydroglaucine and 1,2,9,10-tetramethoxyoxoaporphine, and UV irradiation gives dihydropontevedrine, pontevedrine, glaucine-N-oxide and corunine. These results support the view that glaucine, the main alkaloid in Glaucium flavum, may produce all the more oxidized minor alkaloids present in the plant.     

Lupin alkaloids from sophora chrysophylla

A new lupin alkaloid, (?)-mamanine N-oxide, was isolated from Sophora chrysophylla together with 18 known alkaloids including some unusual lupin alkaloids such as kuraramine, lamprolobine, epilamprolobine, epilamprolobine N-oxide, (+)-mamanine and (?)-pohakuline. It was also shown that the alkaloid constituents of S. chrysophylla differed considerably in the leaves, stems and seeds.