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1.
Phylogeny of the Taxaceae genera and the monotypic family Cephalotaxaceae has been extraordinarily controversial. In this paper chloroplast matK genes and nuclear ITS sequences were determined for all six genera of the two families and representatives of other conifer families. Analysis using either the nonsynonymous sites or the deduced amino acid sequences of matK genes strongly indicates that taxad genera and Cephalotaxaceae are monophyletic, with the Taxodiaceae/Cupressaceae clade as their sister group. Cephalotaxus is basal to the taxad genera, among which two clades, Torreya/Amentotaxus and Taxus/Pseudotaxus/Austrotaxus, are resolved. They correspond to Janchen's two tribes, Torreyeae and Taxeae. In Taxeae, Austrotaxus is the first to branch off. Analyses of the nuclear ITS sequence data corroborated the topology of the matK gene tree. These results refute the views that Cephalotaxaceae has no alliance with Taxaceae and that Austrotaxus and Amentotaxus should be excluded from the Taxaceae. We estimated the divergence time between the Taxodiaceae/Cupressaceae and the Cephalotaxaceae/Taxaceae clades to be 192–230 Myr ago and the divergence time between taxads and Cephalotaxus to be 149–179 Myr ago. Soon after the latter divergence event, within 6–8 Myr, the two taxad tribes originated. In conclusion, our data do not support Florin's claim that taxads could be traced to Devonian psilophytes (359–395 Myr ago).  相似文献   

2.
红豆杉科次生韧皮部的比较解剖   总被引:3,自引:0,他引:3  
在光学显微镜及扫描电镜下,比较观察了红豆杉科Taxaceae5属即红豆杉属Taxus,白豆杉属Pseudotaxus、穗花杉属Amentotaxus,榧树属Torreya和澳洲红豆杉属8种植物茎次生韧皮部的结构。其主要结果为:红豆杉科植物茎次生皮部由轴向系统和径向系统两部分构成。轴向系统由筛胞,韧皮薄壁组织细胞,蛋白细胞及韧皮纤维组成;径向系统由韧皮射线构成,但是,在横切面上,各个组成分子的层次有  相似文献   

3.
通过构建分子钟对广义柏科主要分类群的起源时间进行探讨。采用相对速率检验法分析广义柏科mat K、rbc L进化速率的稳定性,结果显示rbc L的非同义替代速率只在Pinaceae与Taxodiaceae的分类群及柏科北半球的支系(Cupressoideae)之间通过相对速率检验,而Pinaceae与柏科南半球分支(Callitrodeae)之间没有通过相对速率检验。mar K基因的非同义替代速率在Pinaceae与广义柏科的所有分类群之间通过相对速率检验。根据通过相对速率检验的分类群之间的遗传距离和基因进化速率,计算它们发生分歧的时间。据此推测,杉科的主要分类群Taiwanioideae、Athrotaxidoideae、Sequoioideae与其他分支发生分歧的时间均在侏罗纪,支持现存杉科在侏罗纪就已经建立起来的观点;Cupressaceae(s.s.)的两个支系(亚科)发生分歧的时间在124Ma之前,相当于早白垩世早期,可能由于南北古大陆的完全分离,其祖先居群被分隔成两个亚群,随后各自演化为不同的支系。Callitirodeae、Cupressoideae各属发生分歧的时间也均在白垩纪,表明Cupressaceae(s.s.)在白垩纪就已经建立起来。  相似文献   

4.
Reported in the present paper is a robust chloroplast matK gene phylogeny of Taxaceae, Cephalotaxaceae and Podocarpaceae represented by 10 species of seven genera, with three species of the Pinaceae as outgroups. The matk length of the 13 species ranges from 1488 bp to 1548 bp, which results from indels, in particular, 1-bp(base pair) insertion near the 3’ end of the gene in some groups. A 27 bp deletion was found at the nucleotide position 213 from the 5’ end of the matk gene of Pseudotaxus chienii. The aligned sequences used in PAUP and MEGA analyses were 1568 bp and 1494 bp respectively. In the matK gene, the rates of variation at the first, second and third codon positions are similar although the mean frequency of synonymous substitution is approximately twice as high as that of nonsynonymous substitution. Branch-and-Bound search found only one most parsimonious tree (tree length = 895, CI = 0.850, RI = 0. 876), in which all clades were strongly supported by bootstrap test. According to the tree, Taxaceae and Cephalotaxaceae are monophyletic groups, and the sister group relationship between the two families was confirmed. Taxus is closely related to Pseudotaxus while Torreya is the sister group of Amentotaxus. In addition, the close relationship between Nageia and Podocarpus was resolved. The present study supports the generic status of Pseudotaxus and Amentotaxus in point of cladistic analysis and genetic distance, but contra-dicts the establishment of the family Nageiaceae.  相似文献   

5.
The present paper deals with the embryological study and the systematic position of Amentotaxus argotaenia (Hance) Pilger. The material used was collected during 1980-1981 from Jin-fo Shan, 1400-1600 m, Sichuan Province, China. The species is dioecious. The male cone sheds its pollen during the period from the end of May to the middle of June. The pollen at mature stage is 2-celled. Pollen chamber appears obvious at the end of the nucellus. When pollen grains are dispersed, megaspore mother cell, which is situated deep in the nucellus, is in meiosis. The megaspore divides mitotically after pollination and the free nuclei of female gametophyte divide for the last time at the end of June. The wall formation takes place at the stage of 256 free nuclei. The development of archegonia takes place at the beginning of July and the fertilization occurs about July 20-23. The fertilized egg divides successively four times and results in a 16-nucleate proembryo. The young embryo is developing in August. It is interesting to note that the development of the young embryo is very slow. When the seed reaches the mature stage from June to July in the following year, the multicellular masses of the young embryos resulted from simple polyembryony remain immature within the female gametophyte. No cleavage polyembryony has been found. The subsequent embryogeny takes place after the seed has shed. Keng (1975) considers that Amentotaxus links the Taxaceae with Cephalotaxaceae. Our embryological data support Keng’s conclusion since they share (1) compound microstrobilus, (2) 2-celled pollen grains at shedding stage and (3) the rather long life cycle. Keng (1975) also mentions that Podocarpaceae may connect with Taxaceae through Phyllocladus. According to Keng the Podocarpaceae is related to Taxaceae to certain degree. It is obvious that the primitive spike-like male strobilus like the one in Cordaitales is obviously retained in Podocarpus spicatus and P. andinus of Podocarpaceae and Amentotaxus of Taxaceae. In addition, like in Amentotaxus there are 16 nuclei before wall formation in the proembryo of Podocarpus nivalis. These facts may well indicate that at least the Podocarpaceae and the Taxaceae were derived from a common stock. As far as the Taxaceae is concerned the authors tend to support the view of Koidzumi (1932) that Amentotaxus and Austrotaxus should be put in the same tribe since both possess the spike-like strobilus, the long life cycle and the seed maturation in the following year. They are probably rather primitive genera in the Taxaceae. The proembryogeny of Torreya is more or less specialized. It may be placed in a rather advanced tribe and the tribe Taxeae (including Taxus and Pseudotaxus)may be between the above two tribes. In conclusion, the Taxaceae is related to the Coniferales in certain respects and, as Keng (1975), Harri (1976) and Wang et al. (1979) have pointed out recently, placing of the Taxaceae in Coniferales is rather justifiable.  相似文献   

6.
部分裸子植物叶片总蛋白分析   总被引:1,自引:0,他引:1  
王艇  苏应娟  黄超  朱建明   《广西植物》1999,19(4):367-372
采用SDS- PAGE 技术, 分析了红豆杉科(Taxaceae) 植物南方红豆杉( Taxus chinensisvar- mairei (Lemee et Levl-) Cheng et L-K-Fu) 、穗花杉( Amentotaxus argotaenia (Hance) Pil ger) 、云南穗花杉( A- yunnanensis Li) 、白豆杉( Pseudotaxuschienii(Cheng) Cheng) 以及三尖杉科(Cephalotaxaceae) 、植物三尖杉( Cephalotaxus fortunei Hook-f-) 、粗榧( C-sinensis (Rehd-etWils-) Li) 、海南粗榧( C-hainanensis Li) 、篦子三尖杉( C-oliveri Mast-) 和罗汉松科(Podocarpaceae) 、植 物罗汉松 ( Podocarpus macrophyllus ( Thunb- ) D-Don) 、鸡毛 松( P-imbricatus Bl-) 、竹柏( P- nagi(Thunb-) Zoll) 、陆均松( Dacrydium pierrei Hickel) 共12 种植物的叶片蛋白, 在蛋白质水平上采用  相似文献   

7.
苏应娟  王艇 《生态科学》1997,16(1):59-66
采用气相色谱—质谱—计算机联用仪对穗花杉、南方红豆杉、三尖杉和罗汉松叶精油化学成分的研究发现,三尖杉和穗花杉叶精油的组成特点极为相似,相同成分13个,占各自精油组成的48.07%和33.32%.三尖杉和南方红豆杉叶精油的相同成分4个,占各自精油组成的16.14%和40.59%.在一定程度上支持三尖杉科和红豆杉科的亲缘关系接近,红豆杉科可能是通过穗花杉属和三尖杉科相联系的观点.罗汉松和穗花杉叶精油的相同成分4个,占各自叶精油组成的比例为24.09%和20.82%,比罗汉松和南方红豆杉、三尖杉之间组分的相似性要高.反映出罗汉松科和红豆杉科之间有一定联系,穗花杉属是认识红豆杉科、三尖杉科和罗汉松科之间系统关系的关键属  相似文献   

8.
红豆杉科、三尖杉科和罗汉松科植物叶片结构的比较观察   总被引:8,自引:0,他引:8  
扫描电镜和光镜下的叶表皮特征以及叶片解剖结构的研究结果,支持在红豆杉科内建立白豆杉属的处理方式;赞同在三尖杉属内建立篦子三尖杉组,叶片解剖结构方面,三尖杉科和红豆杉科的穗花杉属的相似之处颇多。而叶表皮形态特征方面又表现为三尖杉科和罗汉松科更加接近。反映了出了红豆杉科、三尖杉科和罗汉松科之间的密切而又复杂的系统关系。  相似文献   

9.
The present study deals with pollen morphology of 4 genera and l0 species of Taxaceae in gymnosperms. Pollen grains of the family are spheroidal or subspheroidal, 20.8μm in diameter and with laptoma or papilla in the distal face. Exine is two-layered, with sexine equal to nexine in thickness, but sometimes the stratification is indistinct. The surface is scabrous or slightly granular under LM. Coarse verrucae and fine tuberculae on pollen surface are observed under SEM. From thin section, endexine is shown to have lamellate structure, and ectexine is made of verrucate elements. In Amentotaxus argotaenia, some pollen grains show remnant saccate. According to pollen morphology, this family may be divided into two tribes: 1, Pseudotaxeae (including Pseudotaxus only), and 2, Taxeae (including Taxus and Torreya). Owirg to the special feature of pollen grains in Amentotaxus the present author suggests that the genus be separated from Taxaceae and raised to the level of family, Amentotaxaceae.  相似文献   

10.
A comparative study of Taxus wallichiana Zucc., Cephalotaxus mannii Hook. and Cephalotaxus griffithii Hook. of two families Taxaceae and Cephalotaxaceae has been carried out in detail to support the taxonomic existence of two families. The comparative studies have been carried out on the basis of wood anatomy and palynology. The anatomical properties of wood including the tracheids, ray parenchyma, axial parenchyma and number of cross-field pits have been described in detail. The palynological studies include the shape, size and ultrastructure of pollen grains. These studies give a taxonomic support for the recognition of two different genera of families Taxaceae and Cephalotaxaceae which are closely related.  相似文献   

11.
To determine the evolutionary positions of the conifer genera Amentotaxus, Phyllocladus, and Nageia, we obtained 18S rRNA sequences from 11 new taxa representing the major living orders and families of gymnosperms. With the published Chlamydomonas as an outgroup, phylogenetic analyses of our new data and available sequences indicate that (1) the Gnetales form a monophyletic group, which is an outgroup to the conifers, (2) the conifers are monophyletic, (3) Taxaceae, Cephalotaxaceae, Cupressaceae, and Taxodiaceae form a monophyletic group, (4) Amentotaxus is closer to Torreya than to Cephalotaxus, suggesting that Amentotaxus is better to be classified as a member of Taxaceae, (5) Phyllocladus, Dacrycarpus, Podocarpus, and Nageia form a monophyletic group, and (6) Pinaceae is an outgroup to the other families of conifers. Our finding that Phyllocladus is a sister group of the Podocarpaceae disagrees with the suggestion that the phylloclade of the genus is an ancient structure and that the genus is a terminal taxon within the Podocarpaceae. The genus Nageia is more closely related to Podocarpus than to Dacrycarpus and was derived from within the Podocarpaceae. In conclusion, our data indicate that in conifers, the uniovulate cone occurred independently in Taxacaeae and Cephalotaxaceae, and in Podocarpaceae after the three families separated from Pinaceae, and support the hypothesis that the uniovulate cone is derived from reduction of a multiovulate cone.Correspondence to: S.-M. Chaw  相似文献   

12.
The present investigation was conducted during 1980–1982, and mater- ials collected from Jin-Fo shan (Golden Buddha Mountain), at a height of 1400-1600 m, Sichuan province, China. Pollination of Amentotaxus argotaenia began to proceed last week of May, and came into bloom the first week of June. The male strobiles were almost entirely wilting at June 12–15. Thus, florescence of Amentotaxus spread over a period of 3 weeks. While the pollen grains approaching to maturity, most of the microspores divide to form a larger tube cell and a smaller antheridial initial. In this case the mature pollen grains of Amentotaxus consist of two cells. Then pollen grains are attracted down into the pollen chamber in the apex of the nucellus after pollination. The pollen chamber of Amentotaxus in longitudinal section looks like a flask in shape and is very much similar to that of Ginkgo biloba. As pollen grains at pollen chamber begin to germinate, the antheridial initials divide again to give rise to a spermatogenous cell and a sterile cell. At first, the spermatogenous cell is of a size only 11–13 μ in diameter. When the pollen tube reaches the middle part of the nucellus, the spermatogeneous cell is of a size about 30 μ. In the middle of July, pollen tube approaches the top of the female gametophyte. In this time, the spermatogenous cell has already been mature enough and is of 58–85 μ in diameter. The nuclei of spermatogenous ceils, 30–36 μ in size, are usually lying in the lateral side of the cytoplasm at its micropylar end. From the middle to the end of July, spermatogenous cells divide to form two unequal sperms, one of which is larger than the other and is the functional one. The large sperm is almost round in shape and about 56 μ in diameter. The small sperm is elliptic in shape, non-functional, and about 33 μ in diameter. The nuclei of the large and small sperms are about 40 μ and 26 μ, respectively. In some cases there are lateral pollen tube and sperms in the ovules of Amentotaxus, or the pollen tube even grows toward the lower part of female gametophyte in the chalazal end and there are well developed sperms in such a case. In the middle of July, nucleus of the central cell divides to form a ventral canal nucleus and an egg nucleus. The former then breaks down quickly and the latter continues to develope and moves toward the central part of the egg cell gradually. It is interesting to note that there are a number of nucleolus-like grains in the cytoplasm of the egg cell in Amentotaxus. The large nueleolus-like grains contain a larger central vacuole with several smaller vacuoles surrounding it. These grains show a positive reaction and blue colour by PAS and aniline blue black or coomassie brilliant blue, respectively. The above facts show that the nucleolus-like grains contain not only po- lysaccharides, but also protein. Similar grains may also found in the developing pollen tube. This is a unique feature in Amentotaxus and even in Gymnosperms. Otherwise, there are often two groups of the dense cytoplasm under the egg nucleus in Amentotaxus. Fertilization of Amentotaxus took place around July 20–29 (1980–1982). Interval between pollination and fertilization was about two months. After male nucleus fuses entirely with the female nucleus, the zygote begins to divide by mitosis. During fertilization, in addition that the large sperm enters the egg cell and fuses with the egg nucleus, the small sperm, tube nucleus, and sterile cell are often delivered into the egg cell. But they are disintegrated gradual]y and eventually. It is worthy to note that the nucleolus-like grains and the starches in pollen tube are also released into the egg cell. Then enlargement, fusion, and budding in the nucleolus-like grains may be found within the cytoplasm of the egg cell after fertilization. The history of investigating Amentotaxus found in 1883 has been lasting a long period of 100 years. But researches in sex production has never been studied before. The present work has shown that fertilization in Araentotaxus is very much similar to that in Taxus, Pseudotaxus, and Torreya. In other words, they all belong to the same type, that is, mitosis of zygote taking place after fusion of the two sexual nuclei. This condition constitutes one of the features of Taxaceae. But fertilization in Cephalotaxaceae is different from that of Taxaceae in having mitosis taking place before fusion of the two sexual nuclei. Pollination of Amentotaxus is similar to that of Cephalotaxus with dual-cell pollen grains at shedding stage. On the other hand, interval between pollination and fertilization in Austrotaxus lasts for 13.5 months, and this is the longest one in Taxaceae, and it is similar to that of Cephalotaxus proceeding for 14 months. To sum up, from the point of view of pollination, fertilization, and embryogenesis, Amentotaxus could be considered a primitive type in Taxaceae. Perhaps an order of systematic position of the genera belonging to Taxaceae can be arranged thus: Amentotaxus, Austrotaxus, Taxus, Pseudotaxus, and Torreya. And Cephalotaxaceae may be related to Taxaceae by way of Amentotaxus.  相似文献   

13.
红豆杉科及相关类群rbcL基因PCR—RFLP分析   总被引:3,自引:0,他引:3  
运用RFLP方法对红豆杉科及相关类群14种植物叶绿体rbcL基因PCR产物进行限制酶酶切分析,共获29个酶切变异位点。采用PHYLIP软件包对限制位点变异数据进行极大简约法分析得到18个步长为6的最简约树并求得一致树,结果显示:⑴红豆杉科和三尖杉科属单系群;⑵穗花杉属Amentotaxus以置于红豆杉科内为宜,不支持将穗花杉属独立成科的处理方式;⑶白豆杉应为红豆杉科内一个属Pseudotaxus;⑷三尖杉属内篦子三尖杉地位特殊,可设篦子三尖杉组;⑸不赞同将竹柏类从罗汉松属中分离出去成立新科;⑹红豆杉科、三尖杉科和罗汉松科三者间,前两者的关系更为接近。  相似文献   

14.
运用RFLP方法对红豆杉科及相关类群14种植物叶绿体rbcL基因PCR产物进行限制酶酶切分析,共获29个酶切变异位点。采用PHYLIP 软件包对限制位点变异数据进行极大简约法分析得到18个步长为6的最简约树并求得一致树,结果显示:(1)红豆杉科和三尖杉科属单系群;(2) 穗花杉属Amentotaxus以置于红豆杉科内为宜,不支持将穗花杉属独立成科的处理方式;(3)白豆杉应为红豆杉科内一个属Pseudotaxus;(4) 三尖杉属内篦子三尖杉地位特殊,可设篦子三尖杉组;(5) 不赞同将竹柏类从罗汉松属中分离出去成立新科;(6) 红豆杉科、三尖杉科和罗汉松科三者间,前两者的关系更为接近。  相似文献   

15.
The major peptides in the seed of Taxus and Pseudotaxus have molecular weight about 31, 22 and 20 kilodaltons (Kd) shown by SDS polyacrylamide gel electrophoresis. The seed protein peptides of Cephalotaxus is very similar to those of Taxus and Pseudotaxus except a few bands of high molecular weight. Some considerable differences in peptide pattern exist between Amentotaxus and the three genera cited above. The former has a new major peptide, 33K, but lacks 22 K. The seed of Torreya does not contain peptide 44 K, although Torreya and Amentotaxus have many bands in common. To a certain extent, the seed protein peptides of Podocarpus nagi are similar to those of the above taxa. A great range of divergency in needle peroxidases among different genera of Taxaceae has been observed by using electrophoresis, while the zymogram of Cephalotaxus is somewhat similar to that of Taxus. Two series of protein data demonstrate, that there is an evolutionary tendency from Taxus to Torreya through Pseudotaxus and Amentotaxus within Taxaceae. And the Taxaceae is closely related to Cephalotaxus by way of Taxus. The systematic positionof the Taxaceae, therefore, should be placed under the Coniferales.  相似文献   

16.
Nucleotide sequences from four chloroplast genes, the matK, chlL, intergenic spacer (IGS) region between trnL and trnF, and an intron of trnL, were determined from all species of Taxodiaceae and five species of Cupressaceae sensu stricto (s.s.). Phylogenetic trees were constructed using the maximum parsimony and the neighbor-joining methods with Cunninghamia as an outgroup. These analyses provided greater resolution of relationships among genera and higher bootstrap supports for clades compared to previous analyses. Results indicate that Taiwania diverged first, and then Athrotaxis diverged from the remaining genera. Metasequoia, Sequoia, and Sequoiadendron form a clade. Taxodium and Glyptostrobus form a clade, which is the sister to Cryptomeria. Cupressaceae s.s. are derived from within Taxodiaceae, being the most closely related to the Cryptomeria/Taxodium/Glyptostrobus clade. These relationships are consistent with previous morphological groupings and the analyses of molecular data. In addition, we found acceleration of evolutionary rates in Cupressaceae s.s. Possible causes for the acceleration are discussed.  相似文献   

17.
The genus Cephalotaxus contains a small number of species. It is adequately appreciated as a newly discovered cancerresistant medicament for the alkaloids obtained from its branches leaves and barks are of curative effect. This paper deals with the classificatory revision based on the morphological features, with the reference to the anatomical characters of leaves, types of alkaloids and pollen morphology observed. Two new combinations are proposed, and 4 species and varieties are reduced in the paper. The genus Cephalotaxus is thus suggested to consist of 2 sections and 9 species. The trees occur in East Asia and the north of Indo-China, with 88% found in China where is the distribution centre and refuge of the genus. The genus in discussion is of unique morphological features which are distinctly different from these of Amentotaxus, Cephalotaxaceae, containing a single genus of Cephalotaxus, is closely related to Taxaceae, and therefore the Cephalotaxaceae is best placed in the Taxinieae of Coniferales.  相似文献   

18.
从木材解剖特征初拟针叶树分类系统   总被引:1,自引:0,他引:1  
谢福惠   《广西植物》1982,(4):175-180
<正> 针叶树(Conifers)包括银杏纲和松杉纲的树种。根据《中国植物志》第七卷记载,现代裸子植物的种类分属于4纲9目12科71属约800种,我国产4纲8目11科41属236种,栽培1科7属51种。从国产针叶树材的解剖特征观察,银杏纲木材构造简单,仅具管胞、含晶细胞和射线细胞。管胞排列不整齐,射线薄壁细胞垂直壁无节状加厚,四隅无凹痕,轴向薄壁细胞缺,射线仅单例,所以是针叶村最原始的一个纲,应排列在松杉纲之前。  相似文献   

19.
Nuclear internal transcribed spacer (ITS) regions and chloroplast trnL intron and trnL/trnF spacer and matK sequences were used from 86 accessions to assess relationships among 31 European and South American species of Hypochaeris plus 18 representatives of related genera of tribe Cichorieae. The ITS tree shows high resolution compared to that of the maternally inherited trnL intron, trnL/F spacer, and matK sequences. The ITS and the combined tree reveal clades that agree well with sections of the genus established previously on morphological and cytological grounds, except for H. robertia, which groups with Leontodon helveticus and L. autumnalis. Monophyly of species of Hypochaeris from South America is strongly supported by both ITS and the joint matrix of ITS, trnL, and matK data. European species lie basal to South American taxa, which suggests that species in South America evolved from a single introduction from European progenitors and not from H. robertia as suggested previously. Low levels of sequence divergence among South American taxa suggest a pattern of rapid speciation, in contrast to much greater divergence among European representatives. Different species of Leontodon form two different clades that are also supported by chromosome numbers and morphology. Both nuclear and chloroplast markers suggest that Helminthotheca, Leontodon, and Picris are closely related to each other as well as to Hypochaeris.  相似文献   

20.
Bisflavone constituents of 6 species in the genus Cephalotaxus were analysed by different chemical methods. The result and some suggestions are as follows: 1. Fu's (1984) division of the genus Cephalotaxus into two sections, Cephalotaxus and Pectinatea, is supported by the fact that oliveriflavone has so far been found only in Cephalotaxus oliveri. 2. Our result is favourable to the opinion that Cephalotaxaceae is a natural taxon and includes only one genus, Cephalotaxus, but not to the placement of Amentotaxus of Taxaceae into Cephalotaxaceae. Accroding to the literature and our analytical data, bisflavones and alkaloids are the main constituents of Cephalotaxus, which have not been found in Amentotaxus of Taxaceae. 3. Cephalotaxus is considered closely related to Taxaceae, and Podocarpaceae, but not closely related to Araucariaceae, Pinaceae, Taxodiaceae and Cupressaceae. 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