杉科的细胞分类学和系统演化研究

根据杉科的核型资料,本文(1)提出“1B”可能是一个新的高等植物核型类型;(2)讨论了各属的有关分类学问题及相互亲缘关系,它们的进化顺序可能是柳杉属、水松属、落羽杉属、水杉属、巨杉属、红杉属、杉木属(密叶杉属与之近缘)、台湾杉属;(3)支持金松属分立成金松科,它可能比杉科各属原始; (4)红杉(AAAABB)的亲本可能是二个古代种“水杉”和“巨杉”,它们的直接后裔或留下的近缘是水杉和巨杉;(5)杉科存在A和L两条进化路线,前者包括柳杉属、水松属、落羽杉属、台湾杉属;后者包括水杉属、巨杉属、红杉属、杉木属(密叶杉属);(6)提出一个杉科新系统(包括一个新亚科):Ⅰ.柳杉亚科(柳杉属),Ⅱ.落羽杉亚科(水松属、落羽杉属),Ⅲ.红杉亚科(水杉属、巨杉属、红杉属),Ⅳ.杉木亚科(杉木属、密叶杉属),Ⅴ.台湾杉亚科,新亚科(台湾杉属)。本文还对前人的杉科系统作了讨论。     

从细胞学资料看金松属的系统位置

本文比较了金松(属)和杉科其他各属植物的核型,它的染色体数目(2n=20)和基数(x=10)较低,其核型最为对称。细胞学资料支持金松属从杉科分出另立金松科SciadopityaceaeHayata,它的系统位置则很可能比杉科来得原始。这也得到古植物学的支持。     

杉科的细胞分类学和系统演化研究

根据杉科的核型资料,本文(1)提出“1B”可能是一个新的高等植物核型类型;(2)讨论了各属的有关分类学问题及相互亲缘关系,它们的进化顺序可能是柳杉属、水松属、落羽杉属、水杉属、巨杉属、红杉属、杉木属(密叶杉属与之近缘)、台湾杉属;(3)支持金松属分立成金松科,它可能比杉科各属原始;(4)红杉(AAAABB)的亲本可能是二个古代种水杉”和“巨杉”,它们的直接后裔或留下的近缘是水杉和巨杉;(5)杉科存在A和L两条进化路线,前者包括柳杉属、水松属、落羽杉属、台湾杉属,后者包括水杉属、巨杉属、红杉属、杉木属(密叶杉属);(6)提出一个杉科新系统(包括一个新亚科)：I．柳杉亚科(柳杉属),II．落羽杉亚科(水松属、落羽杉属),III．红杉亚科(冰杉属、巨杉属、红杉属),Ⅳ.杉木亚科(杉木属、密叶杉属),V．台湾杉亚科,新亚科(台湾杉属)。本文还对前人的杉科系统作了讨论。     

密叶杉属的核型分析及其系统位置的探讨

本文首次对特产澳大利亚塔斯马尼亚岛的Athrotaxis cupressoides和Athrotaxis selaginoides进行了核型分析,核型公式分别为2n=22=22m(2SAT)和2n=22=20(2SAT)+2sm,均属Stebbins的1B类型,它们的染色体相对长度组成为22=2L+10M₂+8M_l+2S和22=2L十10M₂+6M_l+4S,后者比前者较为进化。根据密叶杉属和杉科其他各属核型资料的比较分析,它们由原始到进步的顺序可能为：柳杉属、水松属、落羽杉属、水杉属、巨杉属、红杉属,密叶杉属、杉木属和台湾杉属。 密叶属与红杉属、巨杉属和杉木属较为近缘。 这些在以染色体长度比和平均臂比为纵、横坐标的图上得到清楚反映。 根据核型资料,密叶杉属以隶于单型的亚科Arthrotaxoideae较为合适,这也得到形态学、胚胎学、孢粉学和地理学资料的支持。 本文还对前人系统中的密叶杉属位置进行了讨论。     

杉科的两条演化路线

本文根据核型资料提出杉科可能存在A、L两条演化路线,前者包括由原始到进化的柳杉属、水 松属、落羽杉属、台湾杉属,以平均臂比快速增加、染色体长度比缓慢增加为特征;后者包括依序进化的水杉属、巨杉属、红杉属、杉木属(可能还有密叶杉属),以平均臂比缓慢增加、染色体长度比迅速增加为特点。该结论也得到形态学、解剖学、胚胎学等资料的支持。     

新疆猪毛菜属植物染色体数及核型分析

以5种新疆猪毛菜属植物为材料,常规压片法制片后观察记录染色体数,并进行核型分析。实验结果表明:钠猪毛菜体细胞染色体数2n=18;浆果猪毛菜2n=2x=18=12m 6sm,属2A核型;木本猪毛菜2n=2x=18=16m 2sm,属2A核型;东方猪毛菜2n=4x=36=26m 10sm,属2B核型;长刺猪毛菜2n=4x=36=24m 4sm 8st,属2B核型。猪毛菜属植物的染色体基数为9,东方猪毛菜、长刺猪毛菜为四倍体,其它3种均为二倍体。与Бочанцев基于形态学特征建立的分组系统及各组的演化地位相比,东方猪毛菜属于原始的硬叶猪毛菜组,而本研究表明该种在核型上相对较为进化;其余3种核型地位与所属组的演化地位相符。     

桤木属7种植物的核型分析

利用改良去壁低渗法对分布于欧美地区的桦木科(Betulaceae)桤木属(Alnus Mill.)7种植物进行染色体数目与核型分析。结果显示:所有材料染色体形态比较一致,多为由中部(m)及近中部(sm)着丝点染色体组成。意大利桤木(A.cordata)为六倍体,体细胞染色体数为2n=6x=42,核型公式为2n=6x=42=36m+6sm;绿桤木(A.viridis)为八倍体,体细胞染色体数为2n=8x=56,核型公式为2n=8x=56=46m+10sm(SAT);薄叶桤木(A.tenuifolia)、灰桤木(A.incana)、欧洲桤木(A.glutinosa)、裂叶桤木(A.sinuata)和红桤木(A.rubra)均为四倍体,体细胞染色体数均为2n=4x=28,其核型公式分别为2n=4x=28=16m(1SAT)+12sm、2n=4x=28=22m+6sm、2n=4x=28=24m+4sm、2n=4x=28=24m+4sm、2n=4x=28=26m+2sm。其中红桤木(A.rubra)的核型属于1B型,其余均为2B型。     

横断山区伞形科4种7个居群植物的核型研究

对横断山区伞形科棱子芹属2种植物(松潘棱子芹Pleurospermum franchetianumHemsl.和西藏棱子芹Pleurospermum hookeriC.B.Clarke var.thomsoniiC.B.Clarke)和茴芹属2种植物(异叶茴芹Pimpinella diversi-foliaDC.和锐叶茴芹Pimpinella argutaDiels)共7个居群进行体细胞染色体数目观察和核型比较分析,结果表明,棱子芹属和茴芹属植物属内种间染色体基数存在差异,其中松潘棱子芹为2n=2x=18=16sm 2st,西藏棱子芹为2n=2x=22=16m 6sm;茴芹属光果组中锐叶茴芹为2n=2x=22=22m,毛果组中异叶茴芹为2n=18=18st或2n=18=2sm 16st.松潘棱子芹、西藏棱子芹、锐叶茴芹的染色体数目和核型均为首次报道,从而为棱子芹属和茴芹属的分类和演化研究提供细胞学依据.     

中国和邻近地区杉科特有植物的核型及其进化水平的初步研究

中国和邻近地区杉科特有植物的核型类型,柳杉属、水松属、水杉属均为“1A”,杉木属、台湾杉属分别为“1B”和“2B”,它们的进化水平似依序递增并组成A-柳杉属——水松属——台湾杉属和L-水杉属——杉木属二条演化路线。该结果得到某些形态学性状和古植物学的支持,基本上适用于整个杉科。     

横断山及邻近地区八种菊科植物的染色体数目及核型

对横断山及邻近地区风毛菊属(Saussurea)、帚菊属(Pertya)和针苞菊属(Tricholepis)的8种菊科植物进行细胞学研究,其中异叶帚菊(Pertya berberidoides)(2n=2x=32=28m+4sm)、针苞菊(Trichole-pis furcata)(2n=2x=32=16m+ 16sm)、中甸风毛菊(Saussurea dschungdienensis)(2n=2x=30=30m+Bs)、丽江风毛菊(S.likiangensis)(2n 2x=32=26m+6sm)、倒齿风毛菊(S.retroserrata)(2n=2x=32=14m+18sm)和显梗风毛菊(S.peduncularis)(2n=2x=36=26m+ 10sm)为首次报道染色体数目和核型,长毛风毛菊(S.hieracioides)和三角叶风毛菊(S.deltoidea)的核型公式分别为:2n=4x=64=30m+34sm和2n=2x=34=22m+ 12sm,与前人报道的一致.8种植物中,除中甸风毛菊和异叶帚菊的核型不对称性为1B型外,其余6种的核型不对称性均属于2B型;在中甸风毛菊中首次发现B染色体.结合现有的细胞学资料分析表明,风毛菊属和帚菊木族的染色体数目存在变异,并且存在明显的非整倍性;此外,分布于横断山区的风毛菊属植物仪有两种倍性(二倍体和四倍体),而且多倍化并不占主导地位.     

广州地区荷木夜间树干液流补水的影响因子及其对蒸腾的贡献

明确树木夜间水分补充现象有助于提高总蒸腾量和冠层气孔导度估算的精确度,进一步认识冠层蒸腾与树干液流之间存在的时滞关系.本研究采用热消散探针法测定了广州地区的荷木树干液流密度,同步监测了主要的环境因子,从不同时间尺度分析了树干夜间液流的水分补充现象.结果表明：与白天相比,荷木夜间液流密度较小,旱季变化幅度比湿季大;夜间水分补充的时间段主要在前半夜(18:00-22:00);年内各季节夜间水分补充量之间没有显著差异,与环境因子之间的偏相关关系不显著,但与胸径、树高、冠幅、树干生物量、冠层生物量的回归曲线拟合很好,表明树形特征和生物量能更好地解释夜间补水的变化;各季节夜间水分补充量对总蒸腾量的贡献有显著差异,旱季明显高于湿季.     

Head geometric morphometrics of two Chagas disease vectors from Venezuela

Triatominae species are considered the main vectors of Chagas disease or American Trypanosomiasis.In Venezuela,the principal vectors are Rhodnius prolixus (St(a)l,1959) and Triatoma maculata (Erichson,1848),which are belonged to the tribe Rhodniini and Triatomini,respectively.The head conformation and size development of these species can reflect ontogenetic changes which contribute with the vectors biology studies,as well to support of instars determination.The goal of the paper is to the application of geometric morphometric techniques for describing head conformation and size of instars of these species.We photographed 140 heads in R.prolixus:First instar (Ⅰ:16),second instar (Ⅱ:17),third instar (Ⅲ:18),fourth instar (Ⅳ:21),fifth instar (Ⅴ:21),adult female (F:26) and adult males (M:21);in T.maculata heads of 136 specimens were photographed,Ⅰ:20,Ⅱ:17,Ⅲ:26,Ⅳ:15,Ⅴ:19,F:20 and M:19.Landmark coordinate (x,y) configurations were registered and aligned by Generalized Procrustes Analysis.Covariance Analyses were implemented with proportions of re-classified groups and MANOVA.Statistical analyses of variance found not significant differences in head isometric size (Kruskal-Wallis) among Ⅳ and Ⅴ instars in both species.The a posteriori re-classification was almost perfect in R.prolixus (82％) and T.maculata (86％);the main head differences occurs in antenniferous tubercles,postocular and preocular.Our study using quantitative tools for describing the shape differences contributes to explain the morphology variability and development of Chagas disease vectors.     

An Ecogeographical Regionalization for Biodiversity in China

Ecogeographical regionalization is the basis for spatial differentiation of biodiversity research. In view of the principle of international ecogeographical regionalization, this study has applied multivariate analysis and GIS method and based on some ecogeographical attributes limited to the distribution of plant and vegetation, including climatic factors, such as minimum temperature, mean temperature of the coldest month, mean temperature of the wannest month, annual average temperature, precipitation of the coldest month, precipitation of the wannest month, annual precipitation, CV of annual precipitation, biological factors such as vegetation types, vegetation division types, NPP, fiorisitic types, fauna types, abundance of plant species, genus and endemic genus; soil factors such as soil types, soil pH;topographical factors as longitude, latitude and altitude etc. The ecogeographical regionalization for biodiversity in China was made synthetically by using fuzzy cluster method. Four classes of division were used, viz., biodomain, subbiodomain, biome and bioregion. Five biodomains, seven subbiodomains and eighteen biomes were divided in China as follows: Ⅰ Boreal forest biodomain. Ⅰ A Eurasian boreal forest subbiodomain. Ⅰ A1 Southern Taiga mountain cold-temperate coniferous forest biome; Ⅰ A2 North Asian mixed coniferous-broad-leaved forest biome. Ⅱ Northern steppe and desert biodomain. Ⅱ B Eurasian steppe subbiodomain. Ⅱ BI Inner Asian temperate grass steppe biome; Ⅱ B2 Loess Plateau warm-temperate forest/shmb steppe biome. Ⅱ C Asia-Mrica desert subbiodomain. Ⅱ C1 Mid-Asian temperate desert biome; Ⅱ C2 Mongolian/Inner Asian temperate desert biome. Ⅲ East Asian biodomain. Ⅲ D East Asian deciduous broad-leaved forest subbiodomain. Ⅲ D1 East Asian deciduous broad-leaved forest biome, Ⅲ E East Asian evergreen broad-leaved forest subbiodomain. Ⅲ El East Asian mixed deciduous-evergreen broad-leaved forest biome; Ⅲ E2 East Asian evergreen broad-leaved forest biome; Ⅲ E3 East Asian monsoon evergreen broad-leaved forest biome; Ⅲ FA Western East Asian mountain evergreen broadleaved forest biome. Ⅳ Palaeotropical subdomain. IV F India-Malaysian tropical forest subbiodomain.Ⅳ Fl Northern tropical rain forest/seasonal rain forest biome; Ⅳ F2 Tropical island coral reef vegetation biome. Ⅴ Asian plateau biodomain. Ⅴ G Tibet Plateau subbiodomain. Ⅴ G1 Tibet alpine highcold shrub meadow biome;Ⅴ G2 Tibet alpine high-cold steppe biome; Ⅴ G3 Tibet alpine high-cold desert biome; Ⅴ G4 Tibet alpine temperate steppe biome; Ⅴ G5 Tibet alpine temperate desert biome.     

Separation and Identification of Chemical Constituents of Dysosma majorense(Gagn.)Hsiao et Y. H. Chen,nov comb

Ten compounds, namely physcion (Ⅰ), podophyllotoxone (Ⅱ), isopicropodophyllone (Ⅲ), picropodophyllone (Ⅳ), 4'-demethyl-podophyllotoxone (Ⅴ), dehydropodo- phyllotoxin (Ⅵ), diphyllin (Ⅶ), picropodophyllin (Ⅷ), podophyllotoxin (Ⅸ) and 4'-demethylpodophyllotoxin (Ⅹ), were separated from Dysosma majorense (Gagn.) Hsiao et Y. H. Chen, nov comb. Compound Ⅳ was first isolated from natural source and anthraquinone Ⅰ was first isolated from genus Dysosma. Ⅴ, Ⅷ and Ⅹ showed strong acttve inhibited against P388.     

皖琅琊山自然保护区大型真菌群落多样性

对安徽省琅琊山自然保护区大型真菌的群落多样性进行了研究。对该区内设置的样地Ⅰ(针阔混交林)、样地Ⅱ(常绿-落叶阔叶混交林)、样地Ⅲ(落叶阔叶林)、样地Ⅳ(琅琊榆-刺槐林)和样地Ⅴ(竹林)共5种具有代表性的植物群落内的大型真菌的种类和数量进行了调查。选用了物种丰富度(R)、Shannon-Wiener多样性指数(H′)、Pielou均匀度指数(E)和优势度曲线(K-dominance)等指标,对该区大型真菌的群落多样性进行了测定。结果表明,大型真菌的分布与植物群落类型有着密切关系。R的变化趋势为样地Ⅱ样地Ⅰ样地Ⅲ样地Ⅳ样地Ⅴ;H′的变化趋势是样地Ⅰ样地Ⅱ样地Ⅲ样地Ⅳ样地Ⅴ;E的变化趋势是样地Ⅰ样地Ⅲ样地Ⅱ样地Ⅳ样地Ⅴ。另外,季节变化对大型真菌的分布也有较大的影响。秋季大型真菌出现的种类及个体数量较高,R和H′高于春季,而E值却相反。选用的群落多样性指标能较客观地反映该地区大型真菌群落的组成,并揭示不同群落间的关系。     

Studies on the Chemical Constituents of Rourea microphylla (Hook. et Arn) Planch.

Eleven compounds were isolated from the twigs and leaves of Rourea microphylla (Hook. et Arn) Planch. They were identified as quercetin-3-O-α-L-rhamnopyranoside (Ⅰ), hyperin (Ⅱ), quercetin (Ⅲ), astilbin (Ⅳ), β-sitosterol (Ⅴ), β-sitosteryl-β-D-glucopyranoside (Ⅵ), physcion (Ⅶ), erythroglaucin (Ⅷ), stearic acid (Ⅸ), palmitic acid (Ⅹ) and n-nonacosanane (Ⅺ) respectively, by means of UV, IR, NMR, MS spectra analyses and through chemical methods. The compounds Ⅰ, Ⅱ, Ⅲ, Ⅳ, Ⅵ, Ⅶ, Ⅷ, Ⅸ, Ⅹ and Ⅺ were first reportedin the Rourea genus.     

抗性品系棉蚜乙酰胆碱酯酶和羧酸酯酶的变异

用浸叶法测定了采自我国不同地区(泰安、莱阳、南京、北京和安阳)的棉蚜品系Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ对久效磷、甲胺磷、抗蚜威和灭多威等杀虫剂的抗性水平,各棉蚜品系对杀虫剂的抗性依次为Ⅴ>Ⅳ>Ⅲ,Ⅱ>Ⅰ。进一步研究表明,Ⅴ和Ⅳ品系棉蚜乙酰胆碱酯酶对杀虫剂的敏感性显著下降,Ⅱ品系次之,Ⅲ和Ⅰ品系接近于敏感品系。Ⅴ和Ⅳ品系乙酰胆碱酯酶的Km值显著下降,表明酶发生了质的变化。不同棉蚜抗性品系的酯酶（全酯酶和羧酸酯酶）活性均显著升高,其中Ⅲ品系的酯酶活力为Ⅱ品系的2倍。Ⅴ品系羧酸酯酶Km值达2460.4 μmol/L,而Ⅳ品系仅为84.4 μmol/L,该两个品系羧酸酯酶发生了质的变化。研究结果表明,不同抗性程度的棉蚜品系均存在代谢抗性和靶标抗性。低抗水平的棉蚜品系,以代谢抗性为主,靶标抗性为辅;中抗水平的棉蚜品系,抑或由于解毒代谢酶的活性显著增强,也可能由于靶标的敏感性显著下降;而高抗水平的棉蚜品系,依赖于代谢抗性和靶标抗性的联合作用。     

Studies on the Constltuents of the Flavonoids from the Leaves of Typha angustifolia L.

Six flavonoids were isolated from the leaves of Typha angustifolia L. On the basis of spectroscopic (IR, UV, MS, 1HNMR and 13CNMR) analysis, they were identified as quercetin-3,3'-dimethyl ether (TF-Ⅰ), isorhamnetin (TF-Ⅱ), quercetin (TF-Ⅲ), quercetin-3,3' dimethyl ether-4'-O-β-D-glucoside (TF-Ⅳ), isorhamnetin-3-O-β-galactoside (TF-Ⅴ), and isorhamnetin-3-O-neohesperidoside (TF-Ⅵ). Compounds TF-Ⅰ and TF-Ⅴ were found in the genus of Typha for the first time.     

植物组合及水体营养梯度对三种功能性植物生物量累积与分配的影响

设置4个营养水平(I: 0.5 mg N·L^-1, 0.1 mg P·L^-1; II: 1.5 mg N·L^-1, 0.3 mg P·L^-1; III: 4.5 mg N·L^-1, 0.9 mg P·L^-1; Ⅳ: 13.5 mg N·L^-1, 2.7 mg P·L^-1), 研究了水体营养水平、物种组合及其交互作用对入侵漂浮植物凤眼莲、本地扎根浮叶植物黄花水龙和沉水植物苦草生物量累积与分配的影响.结果表明：随营养水平的升高,4个营养水平的凤眼莲和黄花水龙单种和混种的总生物量及茎叶生物量都呈上升趋势,凤眼莲和黄花水龙的总生物量在Ⅲ、Ⅳ处理下平均比Ⅰ、Ⅱ处理下分别增加了54.47%和102.63%;不同植物组合下,苦草各部分生物量呈下降趋势,Ⅲ、Ⅳ处理的总生物量比Ⅰ、Ⅱ处理平均降低了45.88%;经双因素分析,水体营养水平对凤眼莲和黄花水龙生物量有极显著的正影响（P<0.01）,对苦草生物量有极显著的负影响（P<0.01）;而植物组合的影响随目标植物的不 同呈现出差异.