深圳塘朗山郊野公园的植物资源

广东深圳塘朗山郊野公园共有野生维管植物144科423属611种,分别占广东省维管植物280科1589属5737种的51.4%、26.7%和10.65%;其中蕨类省植物21科29属33种,裸子植物3科3属4种,被子植物120科391属574种,被子植物占绝对优势。国家重点保护野生植物共计7科7属7种,占广东省国家重点保护野生植物的10.9%;珍稀濒危植物有4科5属5种,占广东省珍稀濒危植物67种的7%。公园中经济植物可分为12类,分别是药用植物321种,用材树种65种,观赏植物60种,纤维植物41种,野生水果33种,油脂植物38种,饲料植物42种,鞣料植物42种,野菜植物25种,农药植物27种,芳香植物26种,淀粉植物23种,保健植物19种,染料植物13种,有毒植物10种,蜜源植物5种。     

四川唐家河自然保护区鸟类资源

唐家河自然保护区的鸟类已知有204种,分隶于13目40科,占四川省鸟类615种的33%.古北种87种占种数的43%、东洋种90种占种数的44%、广布种27种占种数的13%.特产种27种占全国特产鸟类98种的28%、占四川省特产鸟类59种的46%.国家一级保护鸟类有4种、二级保护有26种,四川省重点保护鸟类有2种,我国和日本国候鸟协定保护的鸟类有22种.区内鸟类生物多样性十分丰富,是候鸟迁徙的重要途经地和停歇地,有候鸟81种,占种数的40%,在鸟类组成中占有比较重要的地位.     

北京市奥林匹克森林公园植物组成分析

奥林匹克森林公园是目前北京市最大的城市公园,自建成以来,奥林匹克森林公园的植物种类组成与来源尚无报道。论文在实地调查数据的基础上,对北京市奥林匹克森林公园的植物组成与分布进行了研究,调查发现园内共有维管束植物295种,隶属于75科,203属,其中乔木种60种,灌木种57种,草本植物170种,藤本8种。按照植物种的自然分布情况统计,发现在园内295种维管束植物中,有北京地区乡土种179种,外来种116种,其中包括外来入侵种4种。按照植物种的来源统计,发现有人工栽种种183种,野生种112种。通过比较分析:发现公园内栽培的本地灌木种占全部栽培灌木种数比例(50.00%)高于整个北京市建成区的比例(27.00%);公园内物种多是国内引进。最后提出了丰富园内野生灌木植物种类;保持乡土种利用;减少对外来种使用等的建议。     

陕西农田蜘蛛的区系分析

陕西农田蜘蛛有32科104属236种,古北界120种,东洋界89种,除上2界外,尚有广泛分布的27种。黄土高原分布区有蜘蛛56种,古北界36种,东洋界3种,广泛分布的17种;关中平原区有蜘蛛135种,古北界78种,东洋界44种,广泛分布的13种;秦岭山区有蜘蛛122种,古北界55种,东洋界50种,广泛分布的17种;汉中、安康盆地区有蜘蛛103种,东洋界66种,古北界26种,广泛分布的11种;大巴山区有蜘蛛16种,东洋界9种,广泛分布的7种。秦岭为2界的分界线,即北纬33°～34°之间分界,此界与陕西等积温(日均温≥10℃)3600℃线吻合,秦岭北为古北界,以南为东洋界,关中平原和汉中、安康盆地区为古北界与东洋界的过渡区。     

内蒙古高原锦鸡儿属植物的形态和生理生态适应性

比较研究内蒙古高原锦鸡儿属(Caragana)中生种,旱生种和强旱生种的叶片形态结构、渗透调节、气孔调节和保护酶,目的是揭示锦鸡儿属不同类型植物的生态适应策略。中生种叶片平展,被稀疏绿色短柔毛;旱生种叶片平展或呈瓦状,被灰色柔毛;强旱生种叶片呈瓦状或卷成筒状,被直立或伏帖绢毛。叶片厚度强旱生种>旱生种>中生种,叶片面积、生物量和比叶面积(SLA)强旱生种<旱生种<中生种。叶片长宽比,强旱生种和旱生种大于中生种。这些形态结构导致保水能力强旱生种>旱生种>中生种,光能利用能力中生种>旱生种>强旱生种。渗透调节物质含量、细胞质离子浓度和细胞渗透势强旱生种>旱生种>中生种。渗透调节物质含量的差异主要表现在强旱生种可溶性糖和无机离子含量远高于旱生种,后者又远高于中生种。叶含水量、自由水含量、叶水势和气孔导度中生种>旱生种>强旱生种,束缚水含量、束缚水/自由水比值、POD和SOD活性正好相反,CAT活性旱生种>中生种>强旱生种。这些生理特性导致抗旱能力强旱生种>旱生种>中生种,但代谢速率正好相反。旱生种和中生种表现出较少的日水分亏缺,强旱生种水分亏缺从清晨到傍晚持续大幅增加。细胞膜相对透性和MDA含量强旱生种>旱生种>中生种。自由基含量表现为旱生种>中生种>强旱生种。这些数据说明虽然旱生种和强旱生种形成了多种特点来适应干旱环境,但仍然是不充分的。结论:(1)分布于半湿润至半干旱区的锦鸡儿属中生种依靠活跃的代谢、大量的水分消耗和快速生长使其在生物环境中取得竞争优势;生活在干旱地区和强干旱地区的旱生种和强旱生种依靠低代谢、节水和高抗旱性来抵抗苛刻的非生物环境。(2) 旱生种和强旱生种主要通过可溶性糖和无机离子的积累,调节细胞质渗透势,保持水分平衡,这是一种相对节省能量的适应对策。     

中国脊椎动物2021年度新增物种报告

为了及时掌握脊椎动物在中国的新增情况, 本文汇总了2021年发表的脊椎动物新物种及新记录种的基本信息。结果表明, 2021年中国新增脊椎动物95种, 包括新种80种, 新记录15种。其中鱼类新种15种、两栖类新种28种、爬行类新种31种和新记录10种、鸟类新种1种和新记录3种、哺乳类新种5种和新记录2种。在新增物种中, 冷血脊椎动物占绝大多数(占总数的88%), 提示这些类群可能仍是以后探索的重点; 两栖类新增物种集中于无尾目、爬行类集中于有鳞目, 分别为27种和40种, 各占其新增物种总数的96%和98%; 新增哺乳类动物全部为小型兽类。本次新增物种的分布涉及30个省区, 其中云南33种、四川11种、广西10种、西藏和广东均为7种、台湾6种, 累计约占新增物种总数的70.5%; 其余省区新增物种在5种或以下。有84个物种(占总数的88%)发表时应用了分子系统学研究, 提示这一技术手段是分类工作的重要支撑。在新发现的95个物种中, 绝大部分物种为中国学者发表; 除3种鸟类新记录种外, 其余的新种和新记录均正式发表于英文期刊, 其中在中国出版的3种期刊发表了21个新种和2个新记录种。本文工作可为中国脊椎动物的分类和保护等相关工作提供基础信息。     

广东省珠海地区蜻蜓目昆虫物种多样性调查

2006～2008年对广东省珠海地区的蜻蜓资源进行调查研究.经过对采集标本的鉴定,珠海地区蜻蜓目昆虫为2亚目7科19属24种,其中2种为广东新记录种,7种为优势种.该地区蜻蜓几的区系特点是:东洋种15种,占总数的50.00%;古北种11种,占总数的36.67%;广布种4种,占总数的13.33%.     

陕西化龙山国家级自然保护区鸟类区系和生态分布

2010年1月至2012年12月采用样线法对化龙山国家级自然保护区鸟类进行了调查。结果表明,保护区有鸟类16目50科224种,占陕西省鸟类种数(475种)的47.16%和全国(1371种)的16.34%。其中,雀形目鸟类32科156种,占69.64%;非雀形目鸟类18科68种,占30.36%。留鸟123种,夏候鸟67种,旅鸟25种,冬候鸟8种,迷鸟1种。在本区繁殖的190种鸟类中,东洋界种100种,古北界种67种,广布种23种。从繁殖鸟的区系成分看,东洋界种与古北界种分别为100种和67种,比例为1.5∶1,东洋界种占优势。从生境分析看,鸟类主要分布于森地和灌草丛。     

四川白蚁名录

为了给基础研究和防治应用提供参考,笔者结合近年的研究成果和经验,对1923~2013年的文献涉及内容进行分析和甄别,确认四川地区(含重庆市)现发现白蚁4科14属96种。其中,草白蚁科:原白蚁属1种;木白蚁科:堆砂白蚁属1种,树白蚁属13种;鼻白蚁科:乳白蚁属1种,散白蚁属39种,杆白蚁属17种;白蚁科:土白蚁属5种,大白蚁属2种,亮白蚁属1种,华扭白蚁属5种,近扭白蚁属3种,象白蚁属4种,钝颚白蚁属3种,新白蚁属1种。四川省发现白蚁4科14属64种:其中草白蚁科:原白蚁属1种;木白蚁科:堆砂白蚁属1种,树白蚁属10种;鼻白蚁科:乳白蚁属1种,散白蚁属23种,杆白蚁属13种;白蚁科:土白蚁属1种,大白蚁属1种,亮白蚁属1种,华扭白蚁属3种,近扭白蚁属2种,象白蚁属4种,钝颚白蚁属2种,新白蚁属1种。     

云南省蝴蝶新纪录种及订正种Ⅰ

报道云南蝴蝶新纪录7种1型及订正种1种的简要形态特征、已知分布区和采集信息.其中新纪录包括凤蝶科1种1型,粉蝶科1种,眼蝶科2种,蛱蝶科1种,灰蝶科2种,订正种为灰蝶科1种.     

Nageiaceae—A New Gymnosperm Family

A new monotypic gymnosperm family, Nageiaceae D. Z. Fu, is separated from Podocarpaceae. It is characterized by having multinerved leaves without costae, and primitive shoot-like female reproductive organs (female strobili). The new family contains a single genus consisting of 2 sections, 5 species and is distributed along the western coast of the Pacific, from low coastal mountains of eastern and southern Asia to the Phillipines and Papua New Guinea. The first species in the Nageiaceae was described as an angiosperm, Myrica nagi Thunb. (1784), but it was soon recognized to be a gymnosperm belonging to a new genus, and was renamed as Nageia japonica Gaert. (1788). The generic name, Nageia, however, has seldom been used, and the members of Nageia have generally been treated as an isolated section of Podocarpus in the Podocarpaceae. When revising the Podocarpaceae, De Laubenfels (1969) established a new genus Decussocarpus based on Nageia, but several years later (1987) he revived the old generic name, Nageia. Page ( 1988,1990)considered Nageia to be a valid generic name and redefined it as a natural genus. The distinctive,broadly lanceolate, multinerved leaves (without costae) of Nageia are rather unusual in gymnosperms,only being similar to those of Agathis in the Araucariaceae, their leaves are also similar to each other in anatomy. For example, there are many single vascular bundles arranged parallelly, between which occur sclerenchyma cells in the mesophyll. Apparently,leaves in Nageia are rather similar both externally and internally to paleogymnosperm cordaitean leaves, and sclerenchyma cells found in Nageia might be the remains of straps between veins in cordaitean leaves. In addition to leaf characters, the large and nearly round pith of the young shoot in Nageia appears to be a reminiscent of the large pith in cordaitean stem. The female reproductive organs (female strobili ) in Nageia are shoot-like. The female strobilus has a sterile terminal bud, and several opposite or subopposite sterile scaly bracts on its axis; two opposite megasporophylls are found near the axis apex and both have an anatropous ovule which is almost entirely covered by the megasporophyll; a bract is partly adnate to the lower back of the megasporophyll;mature arillate seeds are 1-2 or occasionally 3 in number; the axis becomes woody when the seeds mature, but in some species (N. wallichiana) the upper part of the axis becomes fleshy (in the shape of a receptacle), in which no distinct boundary was found between the fleshy receptacle and the woody part, and both have the same scaly bracts or traces. Many characters in Nageia are distinctly different from those in Podocarpus. Leaves in the Podocarpaceae have distinct midribs; in Podocarpus, the reproductive organ, which was generally thought to be similar to that in Nageia, has no terminal bud, and its bract is entirely free from the lower back of the megasporophyll, the fleshy receptacle is derived from both the axis and the sterile bracts (except the lowest two), and the female strobilus at the seed stage has a secondary stalk. The multinerved leaf in Nageia can rarely be found in most of the living gymnosperms except in some rather isolated groups, such as Araucariaceae, Ephedraceae,Ginkgoaceae and Welwitschiaceae. Paleobotanical evidence shows that multinerved leaves have been found in all of the geological ages from the Paleozoic to the present, and such a shoot-like female reproductive organ as in Nageia was found in some paleogymnosperms. It is very difficult to determine the systematic positions of these fossil plants because of lacks adequate material of reproductive organs or even lack of complete vegetative organs. The vascular system and leaf characters of gymnosperms are considered to be very conservative, and the fact that the common leaf shape and venation exist in both fossil and living gymnosperms could imply that there exists a multinerved-leaved evolutionary line ( M-line ) in gymnosperms, which could be traced back to the paleogymnosperm cordaitean plants or even older ones with multinerved leaves. The different types of the female strobili (female reproductive organs) of living gymnosperms, regardless of having one or only several seeds without a typical cone or many seeds with a cone, might have been derived from shoot-like or spikelike female reproductive organs possessed by their common ancestor.The fossil eviden ce shows that the typical cone similar to those of living gymnosperms first appeared in the Jurassic, much later than the single-seeded fossil plant without cones. The seed fossil appeared in the late Devonian Period. It is very difficult to infer the relationships among living gymnosperms, which are hardly derived from one another. But an analysis of the strobili, including the axis structure and position, number, morphology and degree of adnation of the phyllomes on them, would be helpful to the study of their phylogeny. It is evident, therefore, that the gymnosperms with leaves having a midrib might also have a rather long evolutionary course,but no transition between the midrib and multinerved patterns of leaf venation has so far been found in both living and fossil plants. Finally, it is noteworthy that the Nageiaceae are distributed along the western coast of the Pacific, where many primitive representatives, both in gymnosperms and angiosperms, still survive. This would be advantageous to the consideration of Nageiaceae as a primitive representative, or a descendant of fhe paleogymnos-perm cordaitean plants.     

Late Eocene leaves of Nageia (section Dammaroideae) from Maoming Basin,South China and their implications on phytogeography

A new species of Nageia, Nageia maomingensis sp. nov., is described from the Late Eocene of Maoming Basin, Guangdong Province, South China. According to its cuticular characteristics, the present fossil species is assigned to N. sect. Dammaroideae, showing the most resemblance to the extant species N. motleyi (Parl.) de Laub. At present, this section is mainly distributed in the Pacific islands region from South Asia to New Guinea. The discovery of N. maomingensis demonstrates that plants of this section inhabited South China at least by the Eocene. The distribution and living habitat of extant N. sect. Dammaroideae imply that South China was warmer during the Late Eocene than today, and may represent one of the centers for early diversification of Nageia and its section Dammaroideae during the Eocene. In addition, we postulate that plants of sect. Dammaroideae migrated southward in response to climate cooling after the Eocene.     

竹柏类植物的RAPD分析

对鸡毛松（Ｐｏｄｏｃａｒｐｕｓｉｍｂｒｉｃａｔｕｓ）、竹柏（Ｐｏｄｏｃａｒｐｕｓｎａｇｉ）、长叶竹柏（Ｐｏｄｏｃａｒｐｕｓｆｌｅｕｒｙｉ）、百日青（Ｐｏｄｏｃａｒｐｕｓｎｅｒｉｆｏｌｉｕｓ）和罗汉松（Ｐｏｄｏｃａｒｐｕｓｍａｃｒｏｐｈｙｌｕｓ）进行了ＲＡＰＤ分析。经筛选４组８０个引物,发现９个引物的带型清晰并呈多态性。采用ＵＰＧＭＡ法对求出的遗传距离进行聚类分析,得到的结果显示：本研究中的植物明显地分为３个亚类群,支持在罗汉松属内建立竹柏组的处理方式,不同意把竹柏类从罗汉松属中分离出去成立新科的观点     

Phylogeny of Podocarpaceae: comparison of evidence from morphology and 18S rDNA

Maximum parsimony analyses of the genera of Podocarpaceae were conducted using sequence data from 18S ribosomal DNA. Trees from sequence, morphological, and combined data differ in taxon arrangement, but are similar in that Podocarpus sensu lato and Dacrydium s.l. are unnatural, while Podocarpaceae (including Phyllocladus) are monophyletic. The clade Microcachrys + Microstrobos is recognized in all analyses, but its placement differs, i.e., nested among other scale-leaved taxa in the morphological analysis, but associated with Nageia and other tropical genera in the sequence analyses. Trees from combined data reflect this ambiguity. Podocarpus sensu stricto is paraphyletic according to most trees. Inferences of plesiomorphic character states within the family are largely consistent between analyses and support the view that prototypical podocarps had bifacial leaves, cones with several fertile cone scales, and large epimatia (cone scales) that covered the inverted ovules.     

部分裸子植物假种皮微形态特征及其分类学意义

应用扫描电镜对红豆杉科、三尖杉科和罗汉松科植物假种皮的微形态特征进行了研究,结果表明：可以把红豆杉科植物分为两类,即具规则型网状纹饰的红豆杉属和具无规则型网状纹饰的白豆杉属、穗花杉属和榧树属。在后三属中,穗花杉属的穗花杉和白豆杉属的纹饰特征更为相近,同属厚网脊亚型。而云南穗花杉和榧树属的特征相近,属薄网脊亚型。假种皮表面纹饰特征显示不宜将红豆杉（T．chinensis）再分为两个独立的种,认为设立红豆杉和变种南方红豆杉（T．chinensisvar.mairei）的处理方式更加合理。三尖杉科（属）蓖子三尖杉（C．oliveri）假种皮纹饰的网脊、网底分化程度、细胞大小、单位面积细胞数和本届的其它植物差异很大,为建立蓖子三尖杉组提供了进一步的佐证。假种皮的微形态特征还支持把宽叶粗榧（C.sinensisvar.latifolia）上升为种C．latifolia的观点。罗汉松科假种皮纹饰类型的观察结果表明罗汉松属和陆均松属是自然分类群。尽管罗汉松属竹相组假种皮纹饰的网脊变异范围相对较大,但是变异范围仍在属内,不支持将其独立为新科的观点。假种皮的表面纹饰特征还表明三尖杉科和红豆杉科之间的联系密切。     

First fossil record of the genus Nageia (Podocarpaceae) in south China and its phytogeographic implications

The first fossil record of the genus Nageia Gaertner from the Tertiary of southern China is reported. Nageia hainanensis sp. nov. is described from the Eocene Changchang Formation of Hainan Island. The extant species of Nageia are widely distributed in southeastern Asia, from northeastern India to southeastern China and southern Japan, and southward through Indochina to the Malay Archipelago and New Guinea. The fossil evidence of Nageia has been discovered from the Lower Cretaceous of the Far East of Russia and Japan. The distribution of both modern and fossil species of Nageia indicates that this genus could have originated in the northeastern part of Asia in the Early Cretaceous and spread to south China at least in the Eocene. Discovery of Nageia fossil record in south China provides important evidence for the geological and phytogeographic history of the genus.     

Anatomically preserved leaves of the conifer Notophytum krauselii (Podocarpaceae) from the Triassic of Antarctica

Permineralized leaves of the Triassic podocarpaceous conifer Notophytum krauselii are described from the Fremouw Formation of Antarctica. The leaves are elongate and apetiolate with 8-12 parallel veins. The adaxial epidermis consists of rows of rectangular to pentagonal cells; the abaxial epidermis is papillate. Longitudinally oriented stomata occur on both surfaces. An adaxial palisade layer is present and auxiliary sclereids are common in the mesophyll. The vascular bundles have a weakly defined sheath and are flanked by transfusion tracheids. Bundles in the basipetal area of the leaf are capped by sclerotic tissue and subtended by resin canals. These leaves are superficially similar to those of the extant podocarp genus Nageia, but probably represent a distinct acquisition of this leaf type within the Podocarpaceae. Notophytum leaves are similar to the common compression fossil Heidiphyllum elongatum and may be closely related or even conspecific. Evidence from Antarctica suggests that Heidiphyllum and the seed cone Telemachus were produced by the same plant, and may be closely related to several other early Mesozoic conifers with multiveined leaves.     

Chloroplast matK gene phylogeny of Taxaceae and Cephalotaxaceae,with additional reference to the systematic position of Nageia

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.     

Highly rearranged and size‐variable chloroplast genomes in conifers II clade (cupressophytes): evolution towards shorter intergenic spacers

Although conifers are of immense ecological and economic value, bioengineering of their chloroplasts remains undeveloped. Understanding the chloroplast genomic organization of conifers can facilitate their bioengineering. Members of the conifer II clade (or cupressophytes) are highly diverse in both morphologic features and chloroplast genomic organization. We compared six cupressophyte chloroplast genomes (cpDNAs) that represent four of the five cupressophyte families, including three genomes that are first reported here (Agathis dammara, Calocedrus formosana and Nageia nagi). The six cupressophyte cpDNAs have lost a pair of large inverted repeats (IRs) and vary greatly in size, organization and tRNA copies. We demonstrate that cupressophyte cpDNAs have evolved towards reduced size, largely due to shrunken intergenic spacers. In cupressophytes, cpDNA rearrangements are capable of extending intergenic spacers, and synonymous mutations are negatively associated with the size and frequency of rearrangements. The variable cpDNA sizes of cupressophytes may have been shaped by mutational burden and genomic rearrangements. On the basis of cpDNA organization, our analyses revealed that in gymnosperms, cpDNA rearrangements are phylogenetically informative, which supports the ‘gnepines’ clade. In addition, removal of a specific IR influences the minimal rearrangements required for the gnepines and cupressophyte clades, whereby Pinaceae favours the removal of IRB but cupressophytes exclusion of IRA. This result strongly suggests that different IR copies have been lost from conifers I and II. Our data help understand the complexity and evolution of cupressophyte cpDNAs.     

Increases in water potential gradient reduce xylem conductivity in whole plants. Evidence from a low-pressure conductivity method

A new method using hydrostatic suctions (less than 0.02 MPa) was used to measure whole-root conductivity (K(r)) in saplings of two angiosperm pioneer trees (Eucalyptus regnans and Toona australis) and two rainforest conifers (Dacrycarpus dacrydioides and Nageia fleurii). The resultant K(r) was combined with measurements of stem and leaf hydraulic conductivity to calculate whole-plant conductivity and to predict leaf water potential (Psi(l)) during transpiration. At normal soil temperatures there was good agreement between measured and predicted Psi(l) during transpiration in all species. Changes in the soil-to-leaf water potential gradient were produced by root chilling, and in three of the four species, changes in Psi(l) corresponded to those expected by the effect of increased water viscosity on K(r). In one species, however, root chilling produced severe plant wilting and a decline in Psi(l) significantly below the predicted value. In this species Psi(l) decreased to a value close to, or below, the Psi(l) at 50% xylem cavitation. It is concluded that decreased whole-plant conductivity in T. australis resulted from a decrease in xylem conductivity due to stress-induced cavitation.