41 resultados para Ferguson, Kent
Resumo:
早在20世纪三十年代,前人发现山旺中新世具有丰富的植物化石,枝叶、果实、花保存完好。1940年我国植物学家胡先骗与美国加州大学钱耐发表研究专著《中国山东山旺中新世植物群》,报道了30科61属84种植物,为最早系统地进行山旺植物研究的奠基之作,至今仍然具有很高的科学价值和国际影响。1946年布朗发表论文涉及山旺部分属种修订工作。1951年斯行健发表文章:评胡先骗与钱耐著“山东中新统植物群”, 对部分属种鉴定提出异议。1978年植物所与南古所老一辈科学家又作了大量补充与修订,完成合著《中国新生代植物》,该书对山旺植物群进行了系统整理,总计43科87属125种植物,奠定了 山旺植物群的基本面貌。此后,山旺植物群陆续有新的类群添加。目前所知山旺植物群主要以温带落叶植物为主混生了部分亚热带常绿和落叶阔叶植物。该植物群不仅种类繁多,数量丰富,而且保存完整,是我国新生代植物群中研究程度最好的代表。 尽管山旺研究已经取得如此丰富的成果,但是在Hu&Chaney (1940)研究山旺植物群之后的长达60年里( 1940-1999),关于山旺叶、果实与花的研究仅局限于外部的形态描述,缺乏对其进行细胞形态结构和角质层等结构植物学的实验分析研究,从而大大制约了对该植物群性质的理解和类群演化生物学的深入的研究。 近年来我们通过与国际国内同行的广泛合作,运用国际古植物学研究的新技术、新方法,如叶结构分析、角质层分析、细胞形态结构分析等,在光学显微镜与电子显微镜不同层次的观察上,将植物体外部形态学与内部细胞结构研究相结合,开展对山旺植物群的类群研究,取得了重要进展。我们首次成功提取了山旺植物“阿斯羌属”(As tronium)的角质层,并观察到气孔器结构,为该类群的正确修订提供了确凿的生物学证据,建立了化石新属钱耐属(Wang andManchester,2000)。山旺中新世地层中过去报道存在大量的“阿斯羌”花化石,为五个萼片宿存的辐射对称的花,果实球形,一枚,项生。这种生殖结构也普遍见于欧洲大陆的中新世地层和北美大陆美国的始新世地层中。欧洲人Heer在1859年提出它属于分布于东亚的旋花科的飞蛾藤属(Porana)植物; Weyland在1937年认为它应当是热带龙脑香科非洲马达加斯加岛屿特有分布的Mono tes属植物;美国人MacGinitie在1953年认为它属于分布于南美的漆树科的阿斯羌属(Astronium)植物,其确切系统位置众说纷纭。在中国新生代植物一书中,采用了美国人MacGinitie在1953年的观点,称之为阿斯羌花。斯行健先生认为是旋花科的飞蛾藤属植物。 我们调查了密苏里北京植物园标本馆馆藏的南美和非洲标本,以及哈佛大学标本馆的馆藏东亚标本,对上述科属现存植物的花结构进行了全面的详细研究。发现5个萼片宿存的辐射对称的花见于多个不同的科属类群,是一种趋同演化性状,而萼片脉纹与表皮细胞气孔器排列、果实形态与数目等特征在上述不同类群中极易区分。因而逐一排除了属于上述现存类群的可能性。我们研究的山旺与北美的化石标本显示的果实个体发育过程与现存植物苦木科苦木属(Picrasma)的果实发育相似,果实发育早期为5枚分离,后期3-4枚退化,仅1-2枚,通常为1枚球形果实留存,花瓣脱落,萼片宿存。但是,它们二者在果实形态与萼片表皮结构上,仍存在很大差异。现在认为它属于一个绝灭的植物类群,化石的系统位置尚无法放入现存的科属系统,可能接近于苦木科。因此,建立了一个化石新属钱耐属(Chaneya)。目前,该属包含二个种,一个分布于北美始新世地层,另一个分布于东亚中新世地层,欧洲的材料由于缺乏深入研究,尚无法确定归属。钱耐属在北半球第三纪地层中呈东亚北美间断分布。钱耐属的研究,不仅为探讨东亚与北美植物区系的联系和植物类群的分化历史提供了重要的证据(Wang and Manchester,2000),更为深入探讨山旺化石植物重要类群的结构与演化生物学研究提供了成功的范例。 山旺的榉属(Zelkova)是山旺植物群的一个常见分子。榉属是欧亚大陆分布的植物,现存6种,在欧亚大陆第三纪地层中发现了大量的榉属化石,包括果实与叶连生的枝条。在北美大陆虽然有榉属化石报道,但是由于缺乏果实,仅靠叶的特征难以令人信服,榉属是否存在于北美仍有争议( Manchester,1989;Manchester,个人通讯)。近年基于我们在山旺组发现和采集到大量的榉属离散叶片以及联生有果实和叶的生殖枝条的深入研究,获得了化石叶结构、表皮细胞、表皮毛、气孔器、核果的大量结构生物学信息。通过与奥地利维也纳大学的 Ferguson教授合作,建立了欧亚现存榉属6个种的生物学形态与结构信息参照系,古今对比结果清楚表明山旺榉的叶缘齿式结构及表皮特征组合最接近我国南部分布的Z. schneideriana,而不是Hu and Chaney (1940)建议的广布于东亚的Z serrata,也明显不同于欧亚大陆共有、分布于西亚伊朗和东欧高加索地区的Z. carpinifolia。常见于欧洲第三纪的翁格榉(Z. ungeri)在形态学更接近Z.carpinifolia。因此,山旺榉明显不同于翁格榉,有其独立的种级特征,应建立东亚中新世榉属的一新种一山旺榉(Z shanwangensis sp. nov.)。榉属在欧亚大陆上的种级分化可能至少在中中新世即已出现。 我们1995年报道了山旺中新世地层发现中国特有植物杜仲化石,并利用先进的电子显微镜设备,找到了确凿无疑的原位化石杜仲特殊胶丝结构直接证据。《美国植物学报》1997年发表文章评论这是目前我国唯一可靠的、保存有精美的胶丝细胞结构的杜仲化石。近年我们迸一步采用古今结合的方法,运用自创的“特有种气候分析法”,对中国重要特有植物杜仲开展了多学科综合研究,利用现存杜仲种子春季萌发需要特定温度的生理学研究结果,结合自然分布区的温度分布,定量恢复了山旺中新世古春季温度数值;该项研究工作的论文列入著名国际SCI刊物《美国植物学报》2003年1月第一期首篇文章。美国植物学报评审人评价:这是应用现代植物实验数据解决地质时期古气候学问题的一个极好例子,是经典之说“现代是(认知)过去的钥匙”的例证,更是当前古植物学研究的一个范例。该文作出的重要贡献体现在如下几个方面:1、提供了现代植物生理生态的实验数据;2、提供了古植物学研究需要的解剖学证据(胶丝);3、更正了古生物地理方面的一个假说(杜仲何时在中国出现); 4、提出了一个解答古气候学问题的新方法。 最后一点实际上也是最重要的一点。” 油杉属的研究显示该属现代有三个种,生活在东亚中国,越南和老挝。它曾经在北半球广泛分布,以球果、种鳞、具翅的种子、木材等形式保存在新生代第三纪地层中,如已经有报道的北美大陆美国俄勒冈渐新世和中新世,欧洲中部中新世,亚洲日本中新世和上新世,俄罗斯远东渐新世到中新世地层。本次山旺中中新世与美国俄勒冈渐新世Rujada flora发现的油杉,接近现存油杉属的属型种油杉。北美中新世和亚洲日本中新世和上新世报道了接近于现存种铁坚油杉的化石。这些证据反映了东亚与北美第三纪植物区系的联系远比今天密切,油杉在北美中新世末期后、在欧洲早更新世之后和在东亚日本上新世结束,在上述地区消失。油杉今天仅孑遗分布于东亚中国秦岭以南、雅砻江以东,长江以南及台湾、海南岛和越南、老挝等亚热带至热带北缘的低山、丘陵山区。山旺油杉的球果化石具有现存油杉和铁坚油杉复合种的特征,可能代表了兼具中国两种油杉共同特征的一个早期类型,由此也表明油杉和铁坚油杉的物种分化在中国有可能是1500万年以来发生的新近事件。同时,油杉球果(松科)的首次发现,解决了山东山旺中中新世化石产地有无裸子植物这个长达半个世纪的争论(Hu andChaney,1940:斯行健,1951),进一步确证了山旺中中新世气候为亚热带山地气候类型。
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买麻藤纲的系统演化位置数百年来一直是国际植物学界争论的焦点问题。有人认为,买麻藤纲是被子植物的姐妹群,但另有人认为该纲与裸子植物的关系更为密切。尽管存在争议,但是麻黄属(麻黄科)一直被公认为买麻藤纲的基部类群。由于其在植物界中的特殊位置,解剖学、形态和分类学、分子系统学与古植物学等多种学科已经对该属开展了多角度的研究工作。在对买麻藤纲系统发育和演化位置进行研究时,我们意识到麻黄属的历史记录问题不仅是对麻黄属进行其他研究中必须首先解决的关键问题,而且已成为当务之急。而要令人满意的地解决麻黄属的历史记录,必须弄清以下核心问题:①麻黄属的起源时间是什么? ②麻黄属的化石记录怎样? ③早期麻黄植物的多样性怎样? 我们在全世界搜集了麻黄属的全部化石文献,这给我们对该属历史记录进行研究提供了扎实的基础;我们在辽西热河生物群尖山沟组早白垩世地层采集到了保存完好的麻黄化石,这为我们对其历史记录的研究提供了新的材料。 在对该属进行深入的研究后,结合对在中国辽宁省西部尖山沟组早白垩世地层采集到的保存完好的麻黄化石的研究,得出结论如下: (1)麻黄科下原有的似麻黄属和异麻黄属的属征以及模式种的形态特征与麻黄属非常接近。似麻黄属与麻黄属的区别在于二者的时代不同,异麻黄属和麻黄属的差异在于异麻黄属的分枝式样兼具对生和互生。在综合对比后,将似麻黄属和异麻黄属归并入麻黄属中。 (2)根据繁殖器官的特征,对麻黄属下的化石记录进行了整理,结果发现,目前可以确认的麻黄属化石种共有7个,分别是Ephedra chenii (Cao et Wu) Liu, Li et Wang comb. nov., E. antiqua (Heer) Liu, Li et Wang comb. nov., E. xingxuei (Tao et Yang) Liu, Li et Wang comb. nov., E. lanceolata Liu, Ferguson, Li et Wang sp. nov., E. divisa Liu, Ferguson, Li et Wang sp. nov., E. ovata Liu, Ferguson, Li et Wang sp. nov., 以及E. tenera Liu, Li et Wang sp. nov.。其余的种由于性状不明确或缺乏繁殖部分的特征而被暂时搁置一边。 (3)在1.25亿年前,麻黄属在种子单位中苞片的形态、叶片的形态和大小以及叶脉式样等四个方面已经表现出了丰富的多样性。1.25亿年前,麻黄属叶片的最长可达35毫米,最宽可达45毫米,比现代植物的大(最长可达35毫米,最宽可达2毫米);叶片的叶脉式样中在同时具有现在植物的平行脉和汇聚脉之外,还有分叉脉出现。种子单位中苞片的形态主要为鳞片状和披针形,这比现代植物窄;叶片的形态主要有四种类型(卵形、裂叶、披针形以及鳞片状),比现代植物中的两种类型(披针形和鳞片状)复杂。将1.25亿年前多样的麻黄属与现代麻黄植物对比,表明在过去的1.25亿年期间,麻黄属的演化过程为:性状的消失和物种的灭绝。 (4)对于麻黄属的起源时间,对现代麻黄植物叶绿体rbcL基因序列的分析得出的时间为8-32 百万年,而近期基于rbcL、rps4 以及ITS序列和麻黄属化石种子以及麻黄粉的分析,得出麻黄属的起源时间为1.1亿年。我们发现的保存完好的化石标本给出的可靠的直接证据表明,麻黄属植物早在1.25亿年前已经出现,而且当时已经表现出了丰富的多样性,说明麻黄属的起源时间可能会更早。
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美味猕猴桃(Actinidia deliciosa(A.Chev.)C.F.Liang and A.R.Ferguson)和软枣猕猴桃(Actinidia arguta)种间传粉后,花粉管在花柱内行为的荧光观察,以及早期胚胎发生的显微观察,结果如下: 1.花粉粒在柱头的乳头细胞表面萌发,在开放型的V形花柱道内生长。 2.花粉管生长速率比对照缓慢,到达胚珠珠孔的时间平均延迟50到60小时。 3.花粉管在花柱中下部出现形态变化:部分花粉管呈波纹状弯曲;花粉管顶端膨大,尖细或破裂;花粉管直径变化;花粉管解体。 4.花粉管胼胝质沉积的变化:胼胝质沿花粉管壁不规则沉积;有的膨大的花粉管顶端出现胼胝质;有的不出现胼胝质塞,而整个花粉管壁有胼胝质分布,荧光强烈。 5.基于显微结构和种子分析,种间杂交大约有30%的胚珠能够受精,并发育成为种子,种子的胚的大小和胚乳的量与对照有差别,有约70%或更多的表现不育或败育。胚发育为茄型,受精后台子保持休眠十几天后开始横分裂。传粉后七周形成子叶胚。胚发育较对照迟缓。胚乳细胞型。 6.种间杂交能够结实,正常种子占20% -30%,败育干瘪种子占10%左右,未受精胚珠占60%- 70%。种内传粉正常种子占95%,空瘪败育种子占0.7%,未受精胚珠占3.8%。 7.种间杂交果实大小、重量,种子大小及数目,胚的大小都比对照小。
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Domestic cats and dogs are important companion animals and model animals in biomedical research. The cat has a highly conserved karyotype, closely resembling the ancestral karyotype of mammals, while the dog has one of the most extensively rearranged mammalian karyotypes investigated so far. We have constructed the first detailed comparative chromosome map of the domestic dog and cat by reciprocal chromosome painting. Dog paints specific for the 38 autosomes and the X chromosomes delineated 68 conserved chromosomal segments in the cat, while reverse painting of cat probes onto red fox and dog chromosomes revealed 65 conserved segments. Most conserved segments on cat chromosomes also show a high degree of conservation in G-banding patterns compared with their canine counterparts. At least 47 chromosomal fissions (breaks), 25 fusions and one inversion are needed to convert the cat karyotype to that of the dog, confirming that extensive chromosome rearrangements differentiate the karyotypes of the cat and dog. Comparative analysis of the distribution patterns of conserved segments defined by dog paints on cat and human chromosomes has refined the human/cat comparative genome map and, most importantly, has revealed 15 cryptic inversions in seven large chromosomal regions of conserved synteny between humans and cats.
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Forty chromosome-specific paint probes of the domestic dog (Canis familiaris, 2n = 78) were used to delineate conserved segments on metaphase chromosomes of the American mink (Mustela vison, 2n = 30) by fluorescence in situ hybridisation. Half of the 38 canine autosomal probes each painted one pair of homologous segments in a diploid mink metaphase, whereas the other 19 dog probes each painted from two to five pairs of discrete segments. In total, 38 canine autosomal paints highlighted 71 pairs of conserved segments in the mink. These painting results allow us to establish a complete comparative chromosome map between the American mink and domestic dog. This map demonstrates that extensive chromosome rearrangements differentiate the karyotypes of the dog and American mink. The 38 dog autosomes could be reconstructed from the 14 autosomes of the American mink through at least 47 fissions, 25 chromosome fusions, and six inversions. Furthermore, comparison of the current dog/mink map with the published human/dog map discloses 23 cryptic intrachromosomal rearrangements in 10 regions of conserved synteny in the human and American mink genomes and thus further refined the human/mink comparative genome map. Copyright (C) 2000 S. Karger AG, Basel.
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Chromosome homologies between the Japanese raccoon dog (Nectereutes procyonoides viverrinus, 2n = 39 + 2-4 B chromosomes) and domestic dog (Canis familiaris, 2n = 78) have been established by hybridizing a complete set of canine paint probes onto high-res
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We have made a set of chromosome-specific painting probes for the American mink by degenerate oligonucleotide primed-PCR (DOP-PCR) amplification of flow-sorted chromosomes. The painting probes were used to delimit homologous chromosomal segments among human, red fox, dog, cat and eight species of the family Mustelidae, including the European mink, steppe and forest polecats, least weasel, mountain weasel, Japanese sable, striped polecat, and badger. Based on the results of chromosome painting and G-banding, comparative maps between these species have been established. The integrated map demonstrates a high level of karyotype conservation among mustelid species. Comparative analysis of the conserved chromosomal segments among mustelids and outgroup species revealed 18 putative ancestral autosomal segments that probably represent the ancestral chromosomes, or chromosome arms, in the karyotype of the most recent ancestor of the family Mustelidae. The proposed 2n = 38 ancestral Mustelidae karyotype appears to have been retained in some modern mustelids, e.g., Martes, Lutra, ktonyx, and Vormela. The derivation of the mustelid karyotypes from the putative ancestral state resulted from centric fusions, fissions, the addition of heterochromatic arms, and occasional pericentric inversions. Our results confirm many of the evolutionary conclusions suggested by other data and strengthen the topology of the carnivore phylogenetic tree through the inclusion of genome-wide chromosome rearrangements. Copyright (C) 2002 S. KargerAG, Basel.
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Complete sets of chromosome-specific painting probes, derived from flow-sorted chromosomes of human (HSA), Equus caballus (ECA) and Equus burchelli (EBU) were used to delineate conserved chromosomal segments between human and Equits burchelli, and among four equid species, E. przewalskii (EPR), E. caballus, E. burchelli and E. zebra hartmannae (EZH) by cross-species chromosome painting. Genome-wide comparative maps between these species have been established. Twenty-two human autosomal probes revealed 48 conserved segments in E. burchelli. The adjacent segment combinations HSA3/21, 7/16p, 16q/19q, 14/15, 12/22 and 4/8, presumed ancestral syntenies for all eutherian mammals, were also found conserved in E. burchelli. The comparative maps of equids allow for the unequivocal characterization of chromosomal rearrangements that differentiate the karyotypes of these equid species. The karyotypes of E. przewalskii and E. caballus differ by one Robertsonian translocation (ECA5 = EPR23 + EPR24); numerous Robertsonian translocations and tandem fusions and several inversions account for the karyotypic differences between the horses and zebras. Our results shed new light on the karyotypic evolution of Equidae. Copyright (C) 2003 S. Karger AG, Basel.
Resumo:
Conserved chromosomal segments in the black rhinoceros, Diceros bicornis (DB1, 2n = 84), and its African sister-species the white rhinoceros, Ceratotherim simum (CSI, 2n = 82), were detected using Burchell's zebra (Equus burchellii, EBU, 2n = 44) chromosome-specific painting probes supplemented by a subset of those developed for the horse (Equus caballus, ECA, 2n = 64). In total 41 and 42 conserved autosomal segments were identified in C simum and D. bicornis respectively. Only 21 rearrangements (20 fissions and I fusion) are necessary to convert the Burchell's zebra karyotype into that of the white rhinoceros. One fission distinguishes the D. bicornis and C simum karyotypes which, excluding hetero- chromatic differences, are identical in all respects at this level of resolution. Most Burchell's zebra chromosomes correspond to two rhinoceros chromosomes although in four instances (EBU 18, 19, 20 and 21) whole chromosome synteny has been retained among these species. In contrast, one rhinoceros chromosome (DBI1, CSI1) comprises two separate Burchell's zebra chromosomes (EBU11 and EBU17). In spite of the high diploid numbers of the two rhinoceros species their karyotypes are surprisingly conserved offering a glimpse of the putative ancestral perissodactyl condition and a broader understanding of genome organization in mammals. Copyright (C) 2003 S. Karger AG, Base
Resumo:
The Afrotheria, a supraordinal grouping of mammals whose radiation is rooted in Africa, is strongly supported by DNA sequence data but not by their disparate anatomical features. We have used flow-sorted human, aardvark, and African elephant chromosome painting probes and applied reciprocal painting schemes to representatives of two of the Afrotherian orders, the Tubulidentata (aardvark) and Proboscidea (elephants), in an attempt to shed additional light on the evolutionary affinities of this enigmatic group of mammals. Although we have not yet found any unique cytogenetic signatures that support the monophyly of the Afrotheria, embedded within the aardvark genome we find the strongest evidence yet of a mammalian ancestral karyotype comprising 2n = 44. This karyotype includes nine chromosomes that show complete conserved synteny to those of man, six that show conservation as single chromosome arms or blocks in the human karyotype but that occur on two different chromosomes in the ancestor, and seven neighbor-joining combinations (i.e., the synteny is maintained in the majority of species of the orders studied so far, but which corresponds to two chromosomes in humans). The comparative chromosome maps presented between human and these Afrotherian species provide further insight into mammalian genome organization and comparative genomic data for the Afrotheria, one of the four major evolutionary clades postulated for the Eutheria.
Resumo:
With complete sets of chromosome-specific painting probes derived from flow-sorted chromosomes of human and grey squirrel (Sciurus carolinensis), the whole genome homologies between human and representatives of tree squirrels (Sciurus carolinensis, Callosciurus erythraeus), flying squirrels (Petaurista albiventer) and chipmunks (Tamias sibiricus) have been defined by cross-species chromosome painting. The results show that, unlike the highly rearranged karyotypes of mouse and rat, the karyotypes of squirrels are highly conserved. Two methods have been used to reconstruct the genome phylogeny of squirrels with the laboratory rabbit (Oryctolagus cuniculus) as the out-group: ( 1) phylogenetic analysis by parsimony using chromosomal characters identified by comparative cytogenetic approaches; ( 2) mapping the genome rearrangements onto recently published sequence-based molecular trees. Our chromosome painting results, in combination with molecular data, show that flying squirrels are phylogenetically close to New World tree squirrels. Chromosome painting and G-banding comparisons place chipmunks ( Tamias sibiricus), with a derived karyotype, outside the clade comprising tree and flying squirrels. The superorder Glires (order Rodentia + order Lagomorpha) is firmly supported by two conserved syntenic associations between human chromosomes 1 and 10p homologues, and between 9 and 11 homologues.