Dissolution and dispersion of spruce wood components into hot water

Summary The dissolution and dispersion of components from Norway spruce (Picea abies) wood were examined in laboratory experiments to determine the factors influencing variations in dissolved and colloidal substances in mechanical pulp suspensions. Finely ground, fresh spruce wood was suspended in water at 90 °C and was agitated intensively for up to 12 h, after which the concentrations of dissolved and dispersed lipophilic extractives, lignans, carbohydrates and lignins were determined. Sapwood and heartwood were studied separately. Effects of pH and added electrolytes on the dissolution and dispersion of wood components were also investigated.Higher amounts of lipophilic extractives, and especially of triglycerides, were dispersed from sapwood than from heartwood. The release of lipophilic extractives continued for up to 3 h, after which the concentrations in the suspensions leveled off. At this stage the composition of the dissolved and dispersed lipophilic extractives equaled that of the wood. The amount of lipophilic extractives in the suspensions increased with increased pH, in the range of 4.5–6.7, but was lower in the presence of electrolytes. The dissolution of carbohydrates continued even beyond 3 h of agitation. The high water temperature induced hydrolytic reactions, thereby releasing especially arabinose. The release of arabinose through the hydrolytic cleavage from polysaccharides was more extensive at pH 4.5 than at pH 5.5 and 6.7. More polysaccharides containing galacturonic acid units (pectins) were dissolved at a higher pH. Much more polysaccharides containing glucose, most probably starch, were present in the sapwood suspensions. The dissolution of lignins also continued throughout the 12 h experiment. The measured UV-absorption, after extraction of lignans, was roughly the same for sapwood and heartwood suspensions. Slightly less lignins were released in the presence of electrolytes. Lignans were released only from heartwood.     

Wood properties of juvenile and mature heartwood in Robinia pseudoacacia L.

The aim of this study is to characterise the properties of juvenile and mature heartwood of black locust (Robinia pseudoacacia L.). Content, composition and the subcellular distribution of heartwood extractives were studied in 14 old-growth trees from forest sites in Germany and Hungary as well as in 16 younger trees of four clone types. Heartwood extractives (methanol and acetone extraction) were analysed by HPLC-chromatography. UV microspectrophotometry was used to topochemically localise the extractives in the cell walls. The natural durability of the juvenile and mature heartwood was analysed according to the European standard EN 350-1. Growth as well as chemical analyses showed that, based on extractives content, the formation of juvenile wood in black locust is restricted to the first 10–20 years of cambial growth. In mature heartwood, high contents of phenolic compounds and flavonoids were present, localised in high concentrations in the cell walls and cell lumen of axial parenchyma and vessels. In juvenile wood, the content of these extractives is significantly lower. Juvenile wood had a correspondingly lower resistance to decay by Coniophora puteana (brown rot fungus) and Coriolus versicolor (white rot fungus) than mature heartwood.     

Radial variations of vibrational properties of three tropical woods

The radial trends of vibrational properties, represented by the specific dynamic modulus (E′/ρ) and damping coefficient (tan δ), were investigated for three tropical rainforest hardwood species (Simarouba amara, Carapa procera, and Symphonia globulifera) using free-free flexural vibration tests. The microfibril angle (MFA) was estimated using X-ray diffraction. Consistent patterns of radial variations were observed for all studied properties. E′/ρ was found to decrease from pith to bark, which was strongly related to the increasing pith-bark trend of MFA. The variation of tan δ along the radius could be partly explained by MFA and partly by the gradient of extractives due to heartwood formation. The coupling effect of MFA and extractives could be separated through analysis of the log(tan δ) versus log(E′/ρ) diagram. For the species studied, the extractive content putatively associated with heartwood formation generally tends to decrease the wood damping coefficient. However, this weakening effect of extractives was not observed for the inner part of the heartwood, suggesting that the mechanical action of extractives was reduced during their chemical ageing.     

Radial patterns of carbon isotopes in the xylem extractives and cellulose of Douglas-fir

Heartwood extractives (nonstructural wood components) are believed to be formed from a combination of compounds present in the adjacent sapwood and materials imported from the phloem. The roles of local compounds and imported material in heartwood formation could have important implications for the wood quality of species having naturally durable wood. Stable isotope composition (delta(13)C) was analyzed to assess radial variation in sapwood extractives, and to estimate the relative importance of adjacent sapwood extractives and imported photosynthate in the formation of heartwood extractives. Cellulose and extractives from the outer 39 annual rings of six Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) trees were isolated and their delta(13)C composition determined. Although the extractives and the cellulose showed different absolute delta(13)C values, the patterns of change over time (as represented by the annual rings) were similar in most cases. Within an annual ring, carbon isotope ratios of extractives were correlated with the cellulose isotope ratio (R2 = 0.33 in sapwood, R2 = 0.34 in heartwood for aqueous acetone-soluble extractives; R2 = 0.41 in sapwood for hot-water-soluble extractives). These data suggest that some sapwood extractives are formed when the wood ring forms, and remain in place until they are converted to heartwood extractives many years later. Sapwood extractives appear to be important sources of materials for the biosynthesis of heartwood extractives in Douglas-fir.     

Effect of extractives on vibrational properties of African Padauk (<Emphasis Type="Italic">Pterocarpus soyauxii</Emphasis> Taub.)

Extractives can affect the vibrational properties tanδ (damping coefficient) and E′/ρ (specific Young’s modulus), but this is highly dependent on species, compounds, and cellular locations. This paper investigates such effects for African Padauk (Pterocarpus soyauxii Taub.), a tropical hardwood with high extractives content and a preferred material for xylophones. Five groups of 26 heartwood specimens with large, yet comparable, ranges in vibrational properties were extracted in different solvents. Changes in vibrational properties were set against yields of extracts and evaluation of their cellular location. Methanol (ME) reached most of the compounds (13%), located about half in lumen and half in cell-wall. Water solubility was extremely low. tanδ and E′/ρ were very strongly related (R ² ≥ 0.93), but native wood had abnormally low values of tanδ, while extraction shifted this relation towards higher tanδ values. ME extracted heartwood became in agreement with the average of many species, and close to sapwood. Extractions increased tanδ as much as 60%, irrespective of minute moisture changes or initial properties. Apparent E′/ρ was barely changed (+2% to −4%) but, after correcting the mass contribution of extracts, it was in fact slightly reduced (down to −10% for high E′/ρ), and increasingly so for specimens with low initial values of E′/ρ.     

Polyphenols in Acacia mangium and Acacia auriculiformis heartwood with reference to heart rot susceptibility

The heartwood of Acacia mangium is vulnerable to heart rot and this is the first study to investigate the role of heartwood extractives in its susceptibility. Acacia auriculiformis was compared with A. mangium because it is rarely associated with heart rot. The heartwood extracts of both species were dominated by three flavonoids (2,3-trans-3,4′,7,8-tetrahydroxyflavanone, teracacidin, and 4′,7,8,-trihydroxyflavanone), which were purified and identified by nuclear magnetic resonance spectroscopy. The latter compound has not been previously reported in A. mangium and evidence for melacacidin is also newly reported. The mass spectrometric (MS) behavior of these compounds is given, for example teracacidin does not form molecular ions by either electrospray ionization or atmospheric-pressure chemical ionization. The nature of Acacia tannins was compared to quebracho tannin (composed of profisetinidins) using oxidative cleavage to enable MS detection but a negative reaction was obtained for both, which suggests the Acacia tannins may also be of the 5-deoxy proanthocyanidin type. The concentration of flavanones was less when A. mangium heartwood was decayed but the amount of proanthocyanidins was only slightly reduced and therefore these compounds may be more resistant to degradation by heart rot fungi. We found that the total phenol content of A. auriculiformis was about fivefold that of A. mangium, and, while preliminary, this provides evidence for a role played by phenolic extractives in heart rot resistance of these Acacia species.     

Extractives relating to heartwood color changes in sugi (<Emphasis Type="Italic">Cryptomeria japonica</Emphasis>) by a combination of smoke-heating and UV radiation exposure

 Sugi green logs with red or black heartwood were smoke-heated, and the changes in the color of the heartwood after ultraviolet (UV) (λ = 365 nm) radiation exposure were then observed. After UV radiation exposure, the redness and yellowness increased in both the red and black heartwoods, whereas the brightness decreased. In the black heartwood, the resulting color turned from yellowish white to reddish brown. Reddening in black heartwood after exposure to a combination of smoke heating and UV radiation is thought to be due to a decrease in brightness and an increase in both redness and yellowness. However, the degree of change in heartwood color by UV radiation exposure was not greatly affected by smoke-heating treatments of various lengths. When methanol extracts were fractionated and exposed to UV radiation, the yellowness increased in the n-hexane-soluble portion and the redness increased in the acetone-soluble fractions from the n-hexane-insoluble portion. These results suggest that the n-hexane-soluble fraction contains the substances that allow heartwood color to change to yellow after UV radiation exposure, and the acetone-soluble-fraction from the n-hexane-insoluble portion contains the substances that allow it to change to red. Received: November 14, 2001 / Accepted: June 3, 2002 Acknowledgment This research was supported in part by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science. This study was presented in part at the 51st Annual Meeting of the Japan Wood Research Society, Tokyo, April 2001 Correspondence to:N. Yoshizawa     

Residual extractives in aspen kraft pulps and their impact on kappa number and Klason lignin determination

We investigated the impact of residual extractives on lignin determination by lignin content difference between unextracted and extracted pulps, residual extractives analysis, and lignin content contribution from model extractive compounds. There were two different kinds of extractives in aspen kraft pulp. The extractives impacting on kappa number determination were well removed in oxygen delignification; these were mainly unsaturated fatty acids. However, the extractives impacting on Klason lignin determination were largely resistant to oxygen delignification; these were mainly saturated fatty acids, sterols, and hydrocarbons. Oxidation of unsaturated fatty acids was the main reaction in oxygen delignification. These trends were confirmed by simulation of lignin content determination with three model extractive compounds (β-sitosterol, linoleic acid, and palmitic acid). The publication of this article was made possible by an Emachu Research Fund. The authors are grateful for the fund.     

Effect of extractions on dynamic mechanical properties of white mulberry (Morus alba)

Vibrational properties of wood are affected by several parameters, of which extractives can be one of the most important ones. Wood for European musical instruments has been often studied, but traditional Middle Eastern ones had been left unnoticed. In this study white mulberry (Morus alba L.), the main material for long-necked lutes in Iran, was extracted by five solvents of various polarities (water included). Free-free bar forced vibrations were used to measure longitudinal (L) loss tangent (tanδ), storage (elastic) modulus (E′) and specific modulus (E′/γ) in the acoustic range. Their anisotropy between the 3 axes of orthotropy was determined by dynamic mechanical analysis. Native wood had a quite low E _L′/γ but its tanδ was smaller than expected, and the anisotropy of tanδ and E′/γ was very low. Removal of extractives caused tanδ to increase and moduli to decrease. Acetone, the most effective solvent on damping despite a moderate extraction yield, increased tanδ _L by at least 20% but did not modify E′/γ as much. When used successively, its effects masked those of solvents used afterwards. Anisotropy of E′/γ was nearly unchanged after extraction in methanol or hot water, while tanδ was much more increased in R than in T direction. Results suggest that in white mulberry, damping is governed more by nature and localization of extractives rather than by their crud abundance.     

侧柏心材活性成分的提取及其抑菌性能

研究侧柏心材不同部位及正己烷和二氯甲烷依次提取的心材活性成分对白腐菌、褐腐菌、黑曲霉菌的抑菌作用,并采用GC/MS联用技术对提取物中的活性成分进行鉴定和分析.结果表明:侧柏心材从髓心向边材根据年轮所划分的3个部位对3种真菌都具有较好的抑菌效果,并且靠近边材的2部分抑菌效果更明显些.气质联机技术对正己烷和二氯甲烷提取物分析鉴定表明:侧柏心材正己烷提取物中有14种化合物,大部分化合物属于萜烯类物质及其衍生物,最高含量化合物为罗汉柏烯(25.564%)和雪松醇(19.743%);侧柏心材二氯甲烷提取物中鉴定出24种化合物,最高含量化合物也为罗汉柏烯(15.429%).侧柏心材正己烷提取物对褐腐菌、白腐菌和黑曲霉菌第14 d时的抑菌圈直径分别为10.0,9.3和8.3 mm,大于二氯甲烷提取物抑菌圈直径(0,2.7和1.3mm),表明正己烷提取物对3种真菌的抑制生长作用明显优于二氯甲烷提取物的抑菌作用.     

柚木石油醚抽提物成分及其对心边材颜色的影响

为探究国产柚木抽提物对心材和边材颜色差异的影响,采用3种沸程的石油醚溶液分别对国产柚木的心材与边材进行抽提处理,利用气相色谱-质谱法分析抽提液的成分和含量,并以差异较大的抽提物溶液处理柚木边材,通过色度学参数表征柚木边材的变色情况,从而验证影响柚木心材和边材颜色的主要抽提物成分。结果表明:在3种沸程的石油醚抽提液中,柚木心材抽提物在成分种类数量和含量上均显著高于边材;不同沸程的石油醚对柚木心、边材中抽提物成分有一定的影响,其中30~60℃(低沸程)和60~90℃(中沸程)石油醚抽提物成分和含量的差异较小,而90~120℃(高沸程)石油醚抽提物的含量较高,约为中、低沸程抽提物含量的2倍;柚木心材抽提液中酚类、醌类、烯烃类物质的含量较多,但这些物质在边材中含量极低;4-叔丁基-2-苯基苯酚、2-甲基蒽醌(柚木醌)、全反式三十碳六烯(角鲨烯)是柚木心、边材抽提物含量差异最明显的物质。经角鲨烯溶液处理后的柚木边材表面颜色变黄,更接近心材颜色,因此,角鲨烯是导致柚木心边材颜色差异的重要抽提物成分。     

Stereochemistry and biosynthesis of (+)-lyoniresinol,a syringyl tetrahydronaphthalene lignan in <Emphasis Type="Italic">Lyonia ovalifolia</Emphasis> var. <Emphasis Type="Italic">elliptica</Emphasis> II: feeding experiments with <Superscript>14</Superscript>C labeled precursors

To clarify the biosynthetic pathway for syringyl lignans, especially syringyl tetrahydronaphthalene lignans and formation of the C2–C7′ linkage, production of (+)-lyoniresinol (LYR) and its predicted intermediates [syringaresinol (SYR), 5,5′-dimethoxylariciresinol (DMLR), and 5,5′-dimethoxysecoisolariciresinol (DMSLR)] in Lyonia ovalifolia var. elliptica was investigated by means of feeding experiments with radiolabeled precursors. Following individual administration of l-[U-¹⁴C]phenylalanine (Phe), [8-¹⁴C]sinapyl alcohol (SA), and [8,8′-¹⁴C]SYR to excised young shoots of L. ovalifolia and their subsequent metabolism, free [¹⁴C]lignans and [¹⁴C]lignan glycosides were extracted with methanol from stems and leaves and were divided into ethyl acetate-soluble fractions (lignans) and aqueous fractions (lignan glycosides), respectively. Using a combination of xylanase, cellulase, and β-glucosidase, the glycosides were hydrolyzed to liberate [¹⁴C]lignans as aglycones. l-[U-¹⁴C]Phe was incorporated into (+)-[¹⁴C]SYR [stem 0.38%, 8% enantiomeric excess (e.e.)], (−)-[¹⁴C]SYR (leaves 2.75%, 72% e.e.), (+)-[¹⁴C]DMLR (stem 0.07%, 18% e.e. and leaves 0.009%, 58% e.e.), (−)-[¹⁴C]DMSLR (stem 0.03%, 46% e.e. and leaves 0.05%, 20% e.e.), (+)-[¹⁴C]LYR (leaves 0.013%, 22% e.e.) and glycosides of (+)-[¹⁴C]LYR (stem 0.036%, 50% e.e.) in 24h. Based on the percent incorporation and enantiomeric composition of the lignans, the biosynthetic pathway of (8R,8′R)-(+)-LYR was proposed as follows: a nonselective dehydrogenative dimerization of sinapyl alcohol yields (±)-SYR, which is reduced with low specificity to give (8R,8′R)-(+)-DMLR. This is cyclized to directly give (+)-LYR as well as reduced again to (8R,8′R)-(−)-DMSLR. Although further transformation of (−)-DMSLR also leads to the formation of (+)-LYR, cyclization could be a main pathway for (+)-LYR biosynthesis. This report was presented at the IAWPS 2005 International Symposium on Wood Science and Technology, Yokohama, November 2005     

Variation of extractives content in heartwood and sapwood of Eucalyptus globulus trees

The variation in extractives content in sapwood and heartwood was investigated among 12 trees in each of four commercial plantations of Eucalyptus globulus in central Portugal. The study was carried out at the 15% height level and extractions used successively dichloromethane, ethanol and water. At all sites, heartwood had significantly more extractives than sapwood, on average 3.8 and 2.4%, respectively. Most extractives consisted of ethanol soluble material (on average 52% of total extractives). Among the sites, there was a statistically significant difference in the content of extractives but the most important source of variation was the within-tree variation between sapwood and heartwood. Differences in the content of extractives were also observed among trees. A strong relation between extractives content and heartwood proportion was found. The potential loss of pulp yield and problems associated with accumulation of extractives are directly related to the heartwood proportion in the eucalypt stems. Forest management should take into account heartwood development and selection for minimising heartwood extractives.     

Stereochemistry and biosynthesis of (+)-lyoniresinol, a syringyl tetrahydronaphthalene lignan in Lyonia ovalifolia var. elliptica I: isolation and stereochemistry of syringyl lignans and predicted precursors to (+)-lyoniresinol from wood

Steps leading to the biosynthesis of syringyl lignans and tetrahydronaphthalene and naphthalene lignans, especially the formation of the C2–C7′ linkage, have not been elucidated. Lyoniresinol is a typical syringyl lignan, as well as a tetrahydronaphthalene lignan found in Lyonia ovalifolia var. elliptica. To demonstrate the biosynthetic pathway for (+)-lyoniresinol, three putative biosynthetic intermediates of lyoniresinol, syringaresinol, 5,5′-dimethoxylariciresinol, and 5,5′-dimethoxysecoisolariciresinol, were isolated from wood. The identity of the putative intermediates was confirmed by spectroscopic analyses, as well as by comparison of spectral and chromatographic data with those of authentic samples previously synthesized. The stereochemistry (enantiomeric composition and absolute configuration) of the isolated lignans were determined as (±)-syringaresinol, (8S,8′S)-(−)-5,5′-dimethoxylariciresinol [46% enantiomeric excess (e.e.)], (8S,8′S)-(+)-5,5′-dimethoxysecoisolariciresinol (91% e.e.), and (8R,8′R)-(+)-lyoniresinol (42% e.e.). The absolute configurations of (+)-and (-)-5,5′-dimethoxylariciresinols, and (+)-and (-)-5,5′-dimethoxysecoisolariciresinols were determined by their synthesis (catalytic reduction) from (8R,8′R)-(+)-and (8S,8′S)-(-)-syringaresinols and by subsequent chiral high-performance liquid chromatography analysis. This report was presented at the 55th Annual Meeting of the Japan Wood Research Society, Kyoto, March 2005     

Radial distribution of thujaplicins in old growth and second growth western red cedar (Thuja plicata Donn)

Summary Radial distribution of thujaplicins in western red cedar (Thuja plicata Donn) trees of varying ages was studied in order to assess relative decay resistance of their wood. Samples were extracted with ethanol: benzene (1: 2), and the extractives were analyzed for thujaplicin codtent by a new method utilizing capillary gas chromatography of their methylated derivatives. The combined concentration of thujic acid and methyl thujate was also determined for each sample. Distribution of extractives, thujaplicins and thujic acid, generally increased from pith to outside heartwood, then decreased in the sapwood. Maximum extractive and thujaplicin contents were also related to tree age. This suggests that products made from the wood of younger trees will be less resistant to decay than similar products made from the wood of old trees.     

Western red cedar extractives associated with durability in ground contact

Western red cedar (WRC) is well known for its natural durability. However, the roles of all the extractives that may be associated with this durability are not fully understood. The literature primarily credits the thujaplicins, with a lesser role for the lignans; however, previous work has identified highly durable material with low thujaplicin content. To elucidate the relative importance of various extractives, the decay resistance of WRC stakes at four test sites was compared with data on the content of specific extractives to determine whether there was any detectable association. The concentration of plicatic acid, a lignan, was associated with the decay resistance of WRC lumber in ground contact. An unidentified, unquantified compound (B) appeared to be similarly associated with decay resistance. The thujaplicins were only weakly associated with the decay resistance of WRC in ground contact.     

Inhibition activity of essential oils obtained from Japanese trees against <Emphasis Type="Italic">Skeletonema costatum</Emphasis>

The growth inhibition activities of essential oils obtained from Cryptomeria japonica, Chamaecyparis obtusa, and Pinus thunbergii were examined against the bacillariophyceae Skeletonema costatum, also known as red tide plankton. The essential oils were extracted from the heartwood, leaves, and bark of these typical indigenous Japanese conifers. The essential oils from C. japonica bark and P. thunbergii heartwood possessed strong growth inhibition activity. The chemical compositions of these essential oils were analyzed by gas chromatography/flame ionization detection (GC-FID) and gas chromatography/mass spectrometry (GC-MS). α-Terpineol and longifolene were the main components of the essential oil from P. thunbergii heartwood. The C. japonica bark essential oil was mainly composed of α-terpineol, δ-cadinene, isophyllocladene, and ferruginol. Ferruginol and longifolene showed more potent growth inhibition against S. costatum than hinokitiol (β-thujaplicine), which is known to be a strong antifungal compound among wood components. Ferruginol and longifolene were important factors for the growth inhibition activity of the essential oils from C. japonica bark and P. thunbergii heartwood, respectively. These results suggest the possibility of using C. japonica bark and P. thunbergii heartwood for the control of red tide plankton.     

Effects of heartwood extractive fractions of Thuja plicata and Chamaecyparis nootkatensis on wood degradation by termites or fungi

The effect of selective removal of extractives on termite or decay resistance was assessed with matched samples of Thuja plicata Donn ex D. Don and Chamaecyparis nootkatensis (D.Don) Spach heartwood. Samples were extracted using a variety of solvents and then exposed to the subterranean termite Coptotermes formosanus Shiraki in a no-choice feeding test or to the brown-rot fungus Postia placenta (Fr.) M. Larsen & Lombard in a soil bottle test. At the same time, the effect of naturally occurring variations in heartwood extractives on termite or decay resistance was evaluated by testing samples from the inner and outer heartwood of five trees of each species against C. formosanus and P. placenta and analyzing matched wood samples for their extractive content. The results suggest that the methanol-soluble extractives in T. plicata and C. nootkatensis play an important role in heartwood resistance to attack by C. formosanus and P. placenta. Total methanol-soluble extractive content of the heartwood was positively correlated with both termite and decay resistance; however, there was much unexplained variation and levels of individual extractive components were only weakly correlated with one another. Further studies are under way to develop a better understanding of the relationships between individual extractive levels and performance.     

The characterization of wetwood in western hemlock

Summary One of the problem areas in the kiln drying of western hemlock lumber is the wide variation in final moisture content of the wood. This variation in moisture content is due to the presence of sinker or wetwood in the heartwood. The features of wetwood which differentiate it from the normal heartwood include higher specific gravity, higher extractives content, and lower permeability. The apparent higher specific gravity can be fully accounted for by the higher extractives content. The principial extractive is α-conidendrin. The wetwood in western hemlock often occurs together with ring shake and under these circumstances the white deposit on the shake surfaces is also α-conidendrin and not matairesinol, the substance usually associated with ring shake in western hemlock. A viewpoint is presented on the origin of wetwood as the endproduct of a reaction by the tree to injury, i.e., ring shake, in which additional extractives are deposited. The extractives result in a greatly lowered permeability, which prevents loss of moisture during heartwood formation and thereby resulting in wetwood. Bacteria usually found in wetwood and responsible for many of the symptoms associated with wetwood are a result of the high moisture content which favors bacterial growth in wood. Presumably, the two primary sources of loss in kiln drying of western hemlock, shake and wetwood, are often intimately associated. The authors appreciate the assistance of Allen H. Doerksen and Louis W. Hamlin of the Forest Research Laboratory. All samples collected for this study were donated by Willamette Industries, Inc., Dallas, Oregon, and a portion of the research was supported by the Forest Research Laboratory, Oregon State University.     

Analysis of compounds in dichloromethane extractives for Sawara Falsecypress （Chamaecyparis pisifera） outer heartwood

The chemical components of dichloromethane extractives for Sawara Falsecypress heartwood were analyzed with GC/MS except for basic chemical composition analysis for heartwood with Chinese standard method. 14 kinds of compounds were idenfifjed according to the computer compounds library data. The major compounds in dichloromethane extractives comprised of terpene and naphthalene derivafives. The experiments of antifungal effects of the dichloromethane extractive on Aspergillus niger were also carded out. The result showed that the dichloromethane extractive from Sawara Falsecypress has no or weak antifungal capability.