全 文 ：绿槽枝衣的化学成分
周忠玉1 , 3 , 王立松2 , 王 飞1 ,3 , 刘吉开1
?
(1 中国科学院昆明植物研究所植物化学与西部植物资源持续利用国家重点实验室 , 云南 昆明 650204;
2 中国科学院昆明植物研究所生物多样性与生物地理学重点实验室 , 云南 昆明 650204;
3 中国科学院研究生院 , 北京 100049 )
摘要 : 从地衣绿槽枝衣 ( Sulcaria virens) 中分离得到一个新的亚油酸异丙叉衍生物 , 通过波谱学方法包括
2D-NMR 确定其化学结构为 : 9 , 10-O-异丙叉基- (12 Z)-十八碳烯酸 (1)。同时还得到其它 12 个已知化合物 :
( 9 Z, 12 Z )-十八碳二烯酸 (2) , 扁枝衣二酸 (3) , ( R ) -松萝酸 (4) , 枕酸甲酯 ( 5) , 黑茶渍素 (6) , viren-
sic acid ( 7) , abieslactone (8) , 3α-羟基羊毛甾-7 , 24-二烯-26 , 23 R-内酯 (9) , 蒲公英赛醇 (10 ) , 蒲公英赛酮
( 11 ) , (22 E , 24 R )-5α, 8α-过氧麦角甾-6 , 22-二烯-3β-醇 (12) 和 2 , 2′-四氢角鲨烯 (13)。
关键词 : 地衣 ; 绿槽枝衣 ; 化学成分 ; 亚油酸衍生物
中图分类号 : Q 946 文献标识码 : A 文章编号 : 0253 - 2700 (2007) 05 - 586 - 05
Chemical Investigation of Sulcaria virens ( Alectoriaceae)
ZHOU Zhong-Yu1 , 3 , WANG Li-Song2 , WANG Fei1 , 3 , LIU J i-Kai1 *
(1 State KeyLaboratory of Phytochemistry and Plant Resources in West China, Kunming Instituteof Botany, Chinese Academy
of Sciences, Kunming 650204 , China; 2 Laboratory for Plant Biodiversity and Biogeography, Kunming Institute
of Botany, Chinese Academy of Sciences, Kunming 650204 , China;
3 GraduateSchool of the Chinese Academy of Sciences, Beijing 100049 , China)
Abstract: A new linoleic acid derivative, was isolatedfromthe lichen Sulcaria virens together with 12 known compounds .
The structure of the new compound was determined as 9 , 10-O-isopropyllidene -(12 Z)-en-octadecaoic acid (1) by spec-
troscopic analysis . Other 12 known compounds were ( 9 Z, 12 Z ) -octadecadienoic acid ( 2) , evernic acid (3 ) , ( R )-
usnic acid (4) , vulpinic acid ( 5) , atranorin (6 ) , virensic acid (7 ) , abieslactone (8 ) , 3α-hydroxylanosta-7 , 24-dien-
26 , 23 R-olide (9) , taraxerol (10) , taraxerone ( 11 ) , 5α, 8α-epidioxy -( 22 E, 24 R )-ergosta-6 , 22-dien-3β-ol (12 ) ,
2 , 2′-tetrahydrosqualene (13) .
Key words: Lichen; Sulcaria virens; Component; Linoleic acid derivative
Sulcariavirens (Tayl .) Bystr . ex Brodo & Hawk-
sw . belongs to the family Alectoriaceae of lichenized
Ascomyceta (Nash, 1996) , is mainly distributed to the
Himalaya . It is akindof fruticose lichen and its thallus
is bright yellow, corticolous, pendulous ( Awasthi ,
1985) . Previous investigations of lichen in the genus
Sulcaria have reported the isolationof virensic acid, con-
virensic acid, vulpinic acid (Culberson et al . 1981) , and
two depsidons (Elix et al . 1999; Elix et al . 2000) .We
have carried out a detailed chemical investigation on this
lichen and isolated 13 compounds fromits acetoneextracts
including anew linoleic acidderivative, 9 , 10-O-isopro-
pyllidene-( 12 Z) -en-octadecaoic acid (1) . This paper
reports the isolation and structural elucidation of the
new compound . In addition, the1 H- and13 C-NMR da-
ta of 13 were assigned for the first time .
云 南 植 物 研 究 2007 , 29 (5) : 586～590
Acta Botanica Yunnanica

? ?Author for correspondence; Tel : + 86 - 871 - 5216327 ; E-mail : jkliu@ mail .kib. ac. cn
Received date: 2007 - 03 - 21 , Accepted date: 2007 - 07 - 07
作者简介 : 周忠玉 (1982 - ) 女 , 硕士研究生 , 主要从事高等真菌及地衣型真菌化学研究。
Results and Discussion
The 13 compounds from S. virens are mainly
classed to depsides, depsidones, dibenzofuran deriva-
tives and triterpenes, which are abundant in lichen
(Fig . 1) . Compounds2 , 5 and 12 are also often found
in fungi .
Compound 1 was obtained as colorless oil with a
molecular formula C21 H38 O4 . Its
1 H-NMR ( Table 1 )
showed onemethyl atδH 0 .89 (3H, t, J = 7 .0 Hz, H
- 18) , three methylenes atδH 1 .63 (2H, m, H - 3) ,
δH 2 .03 ( 2H, m, H - 14) , δH 2 .35 (2H , t, J = 7 .2
Hz, H - 2) , a double bond atδH 5 .43 (1H, dt, J =
10 .6 , 7 .7 Hz, H - 12) , 5 . 52 ( 1H, dt, J = 10 .6 ,
7 .2 Hz, H - 13) and two methyls atδH 1 .38 (6H, s) ,
which is characteristic of the unsaturated fatty acid de-
rivatives . A quaternary carbon atδC 107 .9 (s, C - 19)
and the methyls protons atδH 1 .38 (6H, s) showed
important correlations in HMBC spectrum ( Fig . 2 ) ,
characteristic of the isopropyllidene moiety . The 13 C-
NMR (Table1 ) of compound 1 showed total 21 carbons
signals, three of which located at the isopropyllidene
moiety, and eighteen of which located at the longchain
unsaturated fatty acid skeleton . In HMBC spectrum of
1 , appearance of key correlations between δH 2 .03
(2H, m, H - 14) andδC 31.5 ( t, C - 16) , δH 0 .89
(3H, t, J = 7 .0 Hz, H - 18 ) andδC 31 .5 ( t, C -
16 ) , but no correlations between olefinic protonδH
5.52 (1H, dt, J = 10 .6 , 7 .2 Hz, H - 13) andδC 31 .5
Fig . 1 Structures of compounds 1 - 13
7855 期 ZHOU Zhong-Yu et al .: Chemical Investigation of Sulcaria virens (Alectoriaceae)
Fig . 2 The key HMBC correlations of compound 1
Table 1 1 H- and 13 C-NMR data for 1 in CDCl3
NO δH δC
1 b179 ?. 1 ( s)
2 b2 ?. 35 ( t, 7 O. 2) 33 k. 9 ( t)
3 b1 ?. 63 ( m) 24 k. 6 ( t)
4 b1 ?. 25 - 1 .36a 29 k. 0 ( t) b
5 b1 ?. 25 - 1 .36a 29 k. 1 ( t) b
6 b1 ?. 25 - 1 .36a 29 k. 2 ( t) b
7 b1 ?. 25 - 1 .36a 26 k. 1 ( t)
8 b1 ?. 51 ( m) 33 k. 0 ( t)
9 b3 ?. 65 ( m) 80 k. 6 ( d)
10 u3 ?. 65 ( m) 80 k. 4 ( d)
11 u2 ?. 33 ( t, 7 O. 7) 30 k. 6 ( t)
12 u5 ?. 43 ( dt, 10 .6 , 7 L. 7) 124 .2 ( d)
13 u5 ?. 52 ( dt, 10 .6 , 7 L. 2) 132 .5 ( d)
14 u2 ?. 03 ( m) 27 k. 4 ( t)
15 u1 ?. 25 - 1 .36a 29 k. 5 ( t) b
16 u1 ?. 25 - 1 .36a 31 k. 5 ( t)
17 u1 ?. 25 - 1 .36a 22 k. 6 ( t)
18 u0 ?. 89 ( t, 7 O. 0) 14 k. 0 ( q)
19 u107 ?. 9 ( s)
20 u1 ?. 38 (s) 27 k. 2 ( q) c
21 u1 ?. 38 (s) 27 k. 3 ( q) c
a Overlapped signals . b, c Assignments maybe interchanged .
( t, C - 16 ) , δH 2 .03 (2H , m, H - 14 ) andδC 22 .6
( t, C - 17) suggested thedoublebond located at C - 12
and C - 13 . The correlations betweenδH 2 .33 (2H , t,
J = 7 .7 Hz, H - 11 ) andδC 80 .6 ( d, C - 9) , 80 .4
( d, C - 10 ) , 124 .2 (d, C - 12) , 132 .5 ( d, C - 13) ,
δH 3 .65 (1H , m, H - 10 ) and olefinic carbon atδC
124 .2 (d, C - 12 ) indicated the isopropyllidene locat-
ed at C - 9 and C - 10 . The Z configuration for the
doublebond was suggested by its coupling constant ( J
= 10.6 Hz) . Thus, the structure of 1 was elucidated
as 9 , 10-O-isopropyllidene-( 12 Z )-en -octadecaoic
acid . Compound 1 seems to be a work-up product of
compound 2 , but when we carried out a reaction of
compound 2 and acetone, compound 1 was failed to be
detected . Inour research, compound 2 wasoften found
in higher fungi , whileisopropyllidenederivativesof fat-
ty acids were not isolated as before .
Experimental
General CC: Column chromatography . TLC: Visualiza-
tion by heating silica-gel plates sprayed with 10% H2 SO4 in
EtOH . Silica gel ( 200 - 300 mesh, Qingdao Marine Chemical
Inc, P . R . China) and Sephadex LH-20 (AmershamBioscienc-
es, Sweden) were used for column chromatography . Pre-coated
silica gel GF-254 plates (Qingdao Marine Chemical Inc, P . R .
China) . Optical rotation: Horiba SEPA-300 spectropolarimeter .
1 H- and 13 C-NMR spectra: Bruker AV-400 and DRX-500 spec-
trometers, δ in ppm, J in Hz . MS: VG Autospec-3000 spec-
trometer, m?z ( rel . int .) .
Lichen Material The fresh lichen thallus were collected
from Laojun Mountains at an altitude of 3 700 m of LijiangCoun-
ty, Yunnan Province, China, on bark of Rhododendron sp . in
June2005 and identified by Wang Li-Song . A voucher specimen
(Wang 05 - 24631 ) was deposited at the Herbarium of Kunming
Institute of Botany, Chinese Academy of Sciences .
Extraction and Isolation The dried lichen thallus ( 180
g) was extracted twice with acetone, then extracted once with
methanol at roomtemperature . The combined extractswere con-
centrated to dryness under reduced pressureto givea residue ( 28
g) which was applied on a silica gel column with a gradient elu-
tion of petroleum ether and acetone (100∶0 , 98∶2 , 95∶5 , 90∶
10 , 80∶20 , 50∶50 , 0∶100) , subsequently seven fractions (A-
G) obtained . Fraction A was further subjected to column chrom-
atography over silica gel ( pure petroleum ether) and Sephadex
LH-20 (CHCl3?MeOH, 1?1) to afford compound 13 (9 .2 mg) .
Fraction B was rechromatographed on Sephadex LH-20 ( CHCl3?
MeOH , 1?1) to give two subfractions, which were recrystallized
to afford pure compounds8 (6 .2 mg) and11 (3.1 mg) . Recrys-
tallization of fraction C and fraction F gave a large amount of
compounds 5 (7 500 mg) and 7 (5 400 mg) , respectively . The
rest of fraction C was further purified with Sephadex LH-20
(CHCl3?MeOH , 1?1) to afford compounds 9 (1 .0 mg) and 10
(0 .8 mg) . Fromthe rest of fraction F , compounds 2 ( 17 .2 mg)
and 3 ( 7 .6 mg) were obtained with repeated chromatography
(CHCl3?MeOH, 125?1 - 60?1) on silica gel column . Thecrystals
from fraction D were rechromatographed on Sephadex LH-20
(CHCl3?MeOH , 1?1) to yield compounds 4 ( 35.5 mg) and 6
885 云 南 植 物 研 究 29 卷
(0 . 6 mg) . Thefraction E was purifiedby repeated silica gel col-
umn ( petroleum ether?acetone, 200?1 - 100?1 ) to give com-
pounds 1 (6 .4 mg) and 12 (9 .1 mg) .
9 , 10-O-isopropyllidene - ( 12 Z )-en-octadecaoic acid
(1) , C21 H38 O4 , colorless oil ; EI-MS m?z ( % ) : 354 [M] +
(25) , 339 (65) , 279 (35) , 243 (100) , 225 (83) , 207 (13) ,
185 (98) , 167 (50 ) , 149 ( 30 ) , 139 ( 37 ) , 121 (52 ) , 95
(27 ) ; 1 H- and 13 C-NMR , Table 1 .
Evernic acid ( 3 ) , C17 H16 O7 ; white powder; FAB-MS
(neg .) m?z: 331 [M-H] - ; 13 C-NMR data ( CD3 COCD3 ) : δC
173 .7 (s) , 170 .3 (s) , 166 .7 (s) , 165 .8 ( s) , 165 .5 (s) ,
144 .7 (s) , 144 .3 (s) , 117 .3 ( d) , 112 .1 ( d) , 111 .3 (s) ,
109 .5 ( d) , 105 .6 (s) , 99 .7 ( d) , 55.9 ( q) , 24.3 ( q) , 23 .9
(q) ; 1 H- and 13 C-NMR data: sameasthe datareported in Narui
et al . (1998) .
( R ) -Usnic acid (4 ) , C18 H16 O7 , yellow needles ( CHCl3?
MeOH ) ; [α] 16D = + 449°( c = 0 .185 , CHCl3 ) ; EI-MS m?z
( % ) : 344 [M] + (45 ) , 260 (55 ) , 233 ( 100) , 217 (25 ) ,
189 (3) , 161 (4 ) ; The data of optical rotation are the same as
reported in Huneck et al . (1976 ) ; MS data are similar to the
data reported in Huneck et al . (1968) .
Vulpinic acid ( 5 ) , C19 H14 O5 , yellow plates ( petroleum
ether?acetone) ; EI-MS m?z ( % ) : 322 [ M ] + ( 20 ) , 290
(80) , 261 (10) , 234 (16) , 178 (15) , 145 (100) , 117 (24) ,
89 (34) , 77 (6 ) , 63 (5 ) ; 13 C-NMR data ( CD3 COCD3 ) : δC
172 .7 (s) , 166 .4 (s) , 161 .6 (s) , 155 .0 ( s) , 133 .4 (s) ,
130 .9 (d, 2×C) , 130 .1 (s) , 129 .16 ( d, 2×C) , 129 .13
(d) , 128.9 ( d) , 128 .7 ( d, 2× C) , 128.3 ( d, 2 ×C ) ,
117 .0 (s) , 104.7 (s) , 55 .0 (q) ; 1 H-NMR data: same as the
datareported in Duncan et al . (2003) ; 13 C-NMR data: same as
the data reported in K?nig et al . (1999) .
Atranorin (6 ) , C19 H18 O8 , colorless needles; EI-MS m?z
( % ) : 374 [M] + (1) , 196 (52) , 179 (13) , 164 (100 ) , 150
(7) , 136 (94 ) , 121 ( 4) , 107 ( 11 ) , 79 ( 9 ) , 67 ( 4) , 53
(3 ) ; MS data are the same as reported in Huneck et al .
(1968) .
Virensic acid (7) , C18 H14 O8 , white powder ; EI-MS m?z
( % ) : 358 [M] + (50 ) , 340 (30 ) , 314 ( 100) , 299 (15 ) ,
285 (20) , 272 ( 36) , 258 ( 70) , 243 ( 40 ) , 230 (50 ) , 190
(8) , 179 (44) ; 13 C-NMR data ( CD3 COCD3 ) : δC 194 .3 (s) ,
174 .0 (s) , 166 .1 (s) , 165 .6 (s) , 161 .6 ( s) , 160 .1 (s) ,
154 .4 (s) , 147.4 (s) , 143.1 (s) , 130 .9 ( s) , 118 .1 ( d) ,
116 .9 (s) , 113 .6 ( s) , 111.8 ( s) , 110 .9 ( s) , 22 .0 ( q) ,
15 .5 ( q) , 9 . 2 (q) ; The data of 1 H- and 13 C-NMR are similar
to those data reported in Elix et al . (2000) .
Abieslactone ( 8 ) , C31 H48 O3 , colorless needles; EI-MS
m?z ( % ) : 468 [M] + ( 5) , 453 ( 14) , 421 (95 ) , 393 (3 ) ,
351 (3) , 325 ( 4 ) , 314 ( 30 ) , 299 ( 22 ) , 227 ( 30 ) , 213
(32 ) , 201 ( 22 ) , 187 ( 78) , 175 (77) , 159 (62) , 147 (71) ,
135 (100) ; 13 C-NMR data ( CDCl3 ) : δC 30 .0 ( t) , 23 .0 ( t) ,
85 .9 ( d) , 37 .6 (s) , 42 .8 (d) , 22 .8 (t) , 121 .6 ( d) , 149 .8
(s) , 48.5 ( d) , 35.7 (s) , 20 .3 ( t) , 35.3 (t) , 43 .7 (s) ,
52 .8 (s) , 33 .2 ( t) , 28 .6 ( t) , 53.9 ( d) , 23 .8 ( q) , 24 .5
(q) , 33.4 (d) , 18 .3 ( q) , 40 .4 (t) , 79.0 (d) , 149.8 ( d) ,
129 .4 (s) , 174.5 (s) , 10.7 ( q) , 23 .8 (q) , 28 .7 ( q) , 30 .9
(q) , 56 .8 (q) ; 1 H- and 13 C-NMR data: same as the data re-
ported in Tkachev et al . (1992) .
3α-Hydroxy-9β-lanosta-7 , 24-dien-26 , 23 R-olide ( 9 ) ,
C30 H46 O3 , colorless needles; EI-MS m?z ( % ) : 454 [ M] +
(6) , 439 (13) , 421 (100) , 403 (3 ) , 314 ( 20 ) , 299 (21 ) ,
281 (14) , 272 (12) , 227 (20) , 213 ( 23) , 201 (15) ; MS and
1 H-NMR data: same as the data reported in Tanaka et al .
(1991) .
Taraxerol (10) , C30 H50 O, colorless needles; EI-MS m?z
( % ) : 426 [M] + ( 7 ) , 411 ( 7 ) , 393 (2 ) , 302 ( 36 ) , 287
(40 ) , 269 ( 23 ) , 257 ( 14) , 245 (8 ) , 231 ( 11 ) , 218 (28 ) ,
204 (100) , 189 (38 ) , 135 ( 52 ) ; MS data are similar to the
datareported in Budzikiewicz et al . ( 1963 ) . 1 H-NMR data:
same as the data reported in Corbett et al . (1972) .
Taraxerone (11) , C30 H48 O, colorless needles; EI-MS m?
z ( % ) : 424 [M] + ( 13 ) , 409 (10) , 300 (70 ) , 285 (59 ) ,
272 (15) , 257 ( 15) , 243 ( 14) , 231 ( 10 ) , 217 (21 ) , 204
(100) , 189 (40) , 133 (73) ; 13 C-NMR data (CDCl3 ) :δC 38 .4
(t) , 34.2 (t) , 217 .5 (s) , 47 .5 (s) , 55 .8 ( d) , 20 .0 ( t) ,
35 .1 ( t) , 38 .9 ( s) , 48 .7 ( d) , 37 .6 ( s) , 17.5 ( t) , 35 .8
(t) , 37 .7 (s) , 157 .6 (s) , 117 .2 ( d) , 36.7 (t) , 37 .7 (s) ,
48 .8 (d) , 40 .7 ( t) , 28 .8 ( s) , 33 .6 ( t) , 33 .1 ( t) , 26 .1
(q) , 21 .5 (q) , 14 .8 ( q) , 29 .9 ( q) , 25 .6 ( q) , 29 .8 ( q) ,
33 .4 ( q) , 21 .4 (q) ; 13 C-NMR data: same asthedata reported
in Sakurai et al . (1987) .
5α, 8α-Epidioxy - (22 E , 24 R )-ergosta-6 , 22-dien-3β-
ol ( 12 ) , C28 H44 O3 , white needles; EI-MS m?z ( % ) : 428
[M] + (1 ) , 410 ( 3) , 396 (8) , 376 (5) , 363 (2) , 337 (2) ,
301 (3) , 285 ( 5 ) , 267 ( 10 ) , 251 ( 20 ) , 161 ( 32 ) , 145
(15 ) , 81 (39) , 69 (100) , 55 (52) ; 1 H- and 13 C-NMR data:
same as the data reported in R?secke et al . (2000 ) .
2 , 2′-Tetrahydrosqualene ( 13 ) , C30 H54 , colorless oil;
EI-MS m?z ( % ) : 414 [M] + (8 ) , 399 (1) , 3290 (4 ) , 301
(15) , 275 (6) , 259 (3) , 233 (5) , 193 (15) , 83 (100) ; 1 H-
NMR data ( CDCl3 ) : δH 0 .87 ( 12H, d, J = 6 .8 Hz, H - 1 , 1′,
13 , 13′) , 1 .51 (2H , m, H - 2 , 2′) , 1 . 14 (4H, q, J = 7 .0
Hz, H - 3 , 3′) , 1 . 37 ( 4H , m, H - 4 , 4′) , 1 .93 (4H, t, J =
7 .6 Hz, H - 5 , 5′) , 5. 10 ( 2H , t, J = 7 .0 Hz, H - 7 , 7′) ,
2 . 09 (4H, q, J = 7 .2 Hz, H - 8 , 8′) , 2 . 00 ( 4H , m, H - 9 ,
9′) , 5 . 15 (2H, br . s, H - 11 , 11′) , 1 . 60 (6H, s, H - 14 ,
9855 期 ZHOU Zhong-Yu et al .: Chemical Investigation of Sulcaria virens (Alectoriaceae)
14′or 15 , 15′) , 1. 58 ( 6H , s, H - 15 , 15′or 14 , 14′) ; 13 C-
NMR data ( CDCl3 ) : δC 22 .7 ( q, C - 1 , 1′, 13 , 13′) , 27 .9
(d, C - 2 , 2′) , 38 .6 ( t, C - 3 , 3′) , 25 .7 ( t, C - 4 , 4′) ,
39 .9 (t, C - 5 , 5′or C - 9 , 9′) , 135 .0 (s, C - 6 , 6′or C - 10 ,
10′) , 124 .0 ( d, C - 7 , 7′) , 26 .6 ( t, C - 8 , 8′) , 39 .8 (t, C
-9 , 9′or C - 5 , 5′) , 135 .3 ( s, C - 10 , 10′or C - 6 , 6′) ,
124 .3 ( d, C - 11 , 11′) , 28 .3 ( t, C - 12 , 12′) , 16 .0 ( q, C -
14 , 14′or C - 15 , 15′) , 15 .9 ( q, C - 15 , 15′or C - 14 , 14′) .
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* * * * * * * * * * * * * * *
《云南植物研究》 征订启事
《云南植物研究》 是国家科委 (79) 国科发条字 341 号文批准创办的植物学专业学报 , 是中国科学院主管的全国
性自然科学期刊。现为我国植物科学研究发表论文的主要学术性刊物之一 , 并被评为“中国自然科学核心期刊”, “中
国生物学类科技核心期刊”。本刊荣获中科院优秀期刊二等奖 (1996 ) 及一等奖 (2000 )、第二届全国优秀期刊三等奖
(1997) 及云南省优秀科技期刊一等奖 ( 1997) 等 , 并作为中国科学院首批向美国 SCI 推荐的刊物之一。并入选国家
“双效期刊”。本刊所发表的论文在国内生物、农林、医药、轻工等二次文献刊物都有摘报 ; 国外 CA (美国化学文
摘)、BA (美国生物学文摘 ) 等从 1980 年起就连续摘报 , 还有生物科学的当代进展 (CABS)、科学引文索引 (SCI ) 的
CI 部分以及俄罗斯文摘杂志 (PЖ) 和国际农业科技情报系统 (Agris) 等摘报。乌利希国际期刊指南 (UIPD) 从 80 年
代就刊载本刊出版事宜。现我刊已同 30 多个国家和地区有发行和交换关系 ; 在国内外同行中有一定的影响。本刊现
已加中国学术期刊光盘版、中国学术期刊网及万方数据库资源系统。
本刊主要报道植物学各分支学科具有创造性或较高学术水平的研究论文和简报 ; 植物学领域的新发现及重大应用
价值的新成果 ; 有关植物学资源开发利用和保护的创新性研究成果 ; 植物学研究的新技术、新方法 ; 反映本学科重要
领域的国内外植物科学研究的最新进展的评述 , 中英文稿件均受欢迎。本刊设有植物系统学与生物地理学、植物化学
与化学生物学、生物多样性保护与民族植物学、植物生态学与资源管理、植物生理与分子生物学 5 个专栏。
《云南植物研究》 为双月刊 , 双月 25 日出版 , 2008 年每期 20 元 , 邮发代号 : 64 - 11 , 若在邮局漏订的读者可直接
与编辑部联系订阅。
联系地址 : 云南昆明市北郊黑龙潭 中国科学院昆明植物研究所 , 邮政编码 : 650204
E - mail: bianji@mail.kib. ac. cn http:?journal.kib. ac. cn Tel & Fax: 0871 - 5223032
095 云 南 植 物 研 究 29 卷