基于线粒体Cyt b,16S rDNA和核28S rDNA的中国斑腿蝗科(直翅目,蝗总科)九亚科间的系统发育关系研究

基于线粒体Cytb、16S rDNA和核28S rDNA的部分序列的联合数据集,重建了中国斑腿蝗科9亚科26种蝗虫和癞蝗科笨蝗(外群)间的系统发育关系。结果显示:1)除黑蝗亚科、秃蝗亚科和切翅蝗亚科外,其余6亚科的单系性都得到支持;2)黑蝗亚科似乎应当与秃蝗亚科合并为一个亚科,且与其他几个亚科亲缘关系相对较远;3)凸额蝗属应该由切翅蝗亚科中独立出来;4)卵翅蝗亚科和稻蝗亚科是姐妹群;5)星翅蝗亚科、黑背蝗亚科、斑腿蝗亚科、刺胸蝗亚科及切翅蝗亚科中的凸额蝗属间的关系较近。     

基于线粒体ND2基因的中国斑翅蝗科部分种类分子系统学研究（直翅目：蝗总科）

本文的目的是通过对斑翅蝗科部分种类的线粒体ND2基因进行分析,重建斑翅蝗科昆虫的系统发育关系,并探讨分子系统发育关系和传统分类结果的异同。扩增并测定了我国斑翅蝗科10属16种蝗虫的线粒体ND2全基因1 023 bp的序列,对序列的碱基组成、转换颠换、系统发育信号等进行了分析。并基于ND2全基因序列数据,分别采用邻接法（NJ）、最简约法（MP）、最大似然法（ML）和贝叶斯法重建了10属16种蝗虫的系统发育关系。结果表明：斑翅蝗科蝗虫ND2全基因A+T含量平均为74.6%;痂蝗亚科和异痂蝗亚科没能得到区分,建议合并为一个亚科;而斑翅蝗亚科和飞蝗亚科的分类地位还存在争议。     

基于线粒体基因Cytb和COI的蝗科中五亚科分子系统发育关系分析（直翅目: 蝗总科）（英文）

本研究基于Cytb 基因和COI基因的部分序列来推断17种蝗虫之间的系统发育关系。这17种蝗虫均采自国内,代表了蝗科(Acrididae)5个亚科：黑蝗亚科(Melanoplinae)、斑腿蝗亚科(Catantopinae)、刺胸蝗亚科(Cyrtacanthacridinae)、斑翅蝗亚科(Oedipodinae)和大足蝗亚科(Gomphocerinae)。采用联合序列方法进行分析,结果显示：Cytb 和COI联合序列长度为1 998 bp,其中A和T总含量为72.13%,G和C总含量为27.87%。联合序列共包含了889个保守位点,1 109个变异位点,在这些变异位点中有838个简约信息位点。系统发生树采用邻接法（NJ）、最大简约法（MP）和最大似然法（ML）进行构建。使用蜢总科的变色乌蜢Erianthus versicolor 和 Erianthus sp. 两个种作为外群。结果表明：大足蝗亚科和斑腿蝗亚科的单系性没有得到支持。斑翅蝗亚科内部各种聚成一个大支,在本研究中该亚科的单系性得到支持,与前人的研究结论相同。大足蝗亚科、斑腿蝗亚科、刺胸蝗亚科和黑蝗亚科这4科关系非常近,可以考虑将其合并为一个亚科。同时,我们发现基于Cytb和COI基因联合序列推断蝗科内各亚科间的系统发生关系并不十分可靠。     

应用16S rDNA序列探讨斑腿蝗科的单系性及其亚科的分类地位

本文测定了斑腿蝗科10亚科20种蝗虫和其他蝗科3种蝗虫的线粒体16S rDNA部分序列,并从GenBank中下载了15种蝗亚目昆虫的16S rRNA基因相应序列片段。比对后的序列长度是397 bp,其中有196个变异位点,157个简约信息位点,A+T平均含量为71.7%,C+G平均含量为28.3%。以序列差异比值为横坐标,以碱基转换数和颠换数为纵坐标作散点图,结果表明颠换多于转换,且随着差异程度的增加,转换明显出现了饱和。以蚱总科的日本蚱Tetrix japonica和卡尖顶蚱Teredorus carmichaeli作外群,用ME、等权MP、加权MP及贝叶斯法重建系统发生树。分子系统树表明,斑腿蝗科并非是一单系群,该科的切翅蝗亚科与稻蝗亚科也均不是一单系群;卵翅蝗、伪稻蝗和稻蝗三者有很近的亲缘关系;支持将黑蝗亚科和秃蝗亚科合为一个亚科——秃蝗亚科;现行的稻蝗亚科并非一单系群,而是一多系群。分子系统学研究结果和传统的基于形态特征的斑腿蝗科的分类体系有很大的不同。     

蝗科高级阶元的分子系统发育(英文）

迄今,蝗科内各分类阶元之间的系统发生关系大部分是未知的。本文用来自中国24种蝗科昆虫的12SrDNA和16SrDNA2个基因的联合序列(共795bp)数据,以锥头蝗科的锥头蝗(Pyrgomorpha conica)为外群,重建了分子系统树。研究结果表明,在12SrDNA与16SrDNA组成的联合数据中,转换的替代速率明显比颠换的替代速率高得多,核酸的替代已经发生了饱和。分子系统树表明:斑翅蝗亚科是一单系群,该亚科是一个合法的亚科,但斑腿蝗亚科和蝗亚科都不是单系群;斑翅蝗亚科在蝗科内是一个相对原始的类群,而稻蝗亚科比斑翅蝗亚科相对进化,比蝗科的其他亚科的种类相对原始。     

中国蝗总科昆虫科间系统发育关系支序分析：直翅目;蝗亚目

在形态学研究的基础上,配方选择了１２个特征,利用Ｈｅｎｎｉｇ８６程序包,以支序分析探讨了中国蝗总科昆虫科间的系统发育关系。结果表明蝗虫类昆虫稳定的分为两大类,即癞蝗类和蝗类,本文建议蝗虫类昆虫分为分为两个总科较宜。长腹蝗亚科似归入斑腿蝗亚科更为合理;而皱腹亚科则应提升为独立科。     

欧亚大陆斑翅蝗科分类系统(直翅目: 蝗亚目)

对分布在欧亚大陆的斑翅蝗科Oedipodidae昆虫进行了亚科分类研究, 将已知的69个属分为7个亚科: 飞蝗亚科Locustinae, 斑翅蝗亚科Oedipodinae, 异距蝗亚科Heteropterninae subfam. n., 痂蝗亚科Bryodeminae, 异痂蝗亚科Bryodemellinae, 哑斑翅蝗亚科Oedipodacrinae subfam. n.和聋斑翅蝗亚科Rashidinae subfam. n., 其中包括3个新亚科。建立了欧亚大陆斑翅蝗科新的亚科分类系统。     

基于COⅡ基因序列的斑腿蝗科部分亚科的分子系统学研究

采用PCR产物直接测序法测定了斑腿蝗科10个亚科16属22种的COⅡ基因585 bp的片段, 对序列的碱基组成进行了分析,并评估了数据集的系统发育信号;最后,以癞蝗科的肃南 短鼻蝗作为外群,采用NJ法、MP法、ML法以及贝叶斯推论法构建了系统树,以解决这些物种所代表的亚科之间的系统发育关系。结果表明：22种斑腿蝗科昆虫的COⅡ基因序列碱基组成表现强烈的A+T含量偏向性。对COⅡ基因585 bp序列片段构成的全数据组和根据密码子不同位点划分的密码子第一、第二和第三位点数据组的系统发育信号分析显示,所有数据组都具有一定的系统发育信息。在4种方法得到的合一树中发现： （1）星翅蝗亚科、刺胸蝗亚科、黑背蝗亚科、斑腿蝗亚科的亲缘关系较近;（2）卵翅蝗亚科与稻蝗亚科亲缘关系较近,建议卵翅蝗亚科似乎应归入稻蝗亚科中,板胸蝗亚科与这两个亚科的关系较近;（3）黑蝗亚科和秃蝗亚科似乎应合并为一个亚科;（4）切翅蝗亚科的4个属未聚在一起,表明这些属的区别较大,不是一个单系群;（5）黑蝗亚科和秃蝗亚科关系较近,且与本研究中其他几个亚科的亲缘关系相对较远。研究结果表明COⅡ基因在解决斑腿蝗科的亚科以下属种间的系统发育关系时是一个有效的分子标记。     

湖南蝗虫三新种（直翅目：蝗总科

记述采自湖南省山区的蝗虫３新和 山卵翅蝗Ｃａｒｙａｎｄａ ｊｉｕｙｓｈａｎａ,ｓｐ．ｎｏｖ．（斑腿蝗科Ｃａｔａｎｔｏｐｉａｄａｅ卵翅蝗属Ｃａｒｙａｎｄａ ｓｔａｌ,１８７８）, Ｆｒｕｈｓｔｏｒｆｅｒｉｏｌａ ｘｕｅ ｆｅｒｎｓｈａｎａ,ｓｐ．ｖｏｎ．（斑腿蝗科Ｃａｔａｎｔｏｐｉｄａｅ腹露蝗属Ｆｒｕｈｓｔｏｒ ｆｅｒｉｏｌａＷｉｌｌｅｍｓｅ,１９９２）,大围山雏蝗Ｃｈｏｒｔｈｉｐｐｕｓ ｄａｗｅｉ     

斑腿蝗科精小管形态及其分类学意义探讨

首次对斑腿蝗科 3 5属 4 6种的精小管形态进行了度量描记 ,并应用SPSS软件对上述种类的精小管量度作了统计分析。结果表明 ,斑腿蝗科精小管形态在属内种间具有稳定性 ,在亚科级阶元具有其各自的特征 ,可作为亚科间比较的一项有用指标。其中 ,稻蝗亚科精小管较短小 ,接近于蚱总科及蝗总科癞蝗科等原始类群 ,显示其原始性 ;板胸蝗亚科较为进化并与秃蝗、裸蝗亚科具较近亲缘关系。斑腿蝗亚科各属间精小管形态变异较大 ,但以梭形至杆状为主 ,显示其较进化的特点。本文结果初步表明 :作为一个方面的分类学性状 ,蝗虫精小管形态可以作为属上高级阶元的比较特征。     

Reconstruction of phylogeny of locusts from the family Acrididae (Orthoptera) based on analysis of nucleotide sequences of 16S ribosome RNA gene in mitochondria

The sequences of two mitochondrial 16S RNA gene fragments (137- and 174-bp in size) were determined in nine grasshopper species belonging to three Acrididae subfamilies. Phylogenetic reconstruction was performed using the sequences of twelve grasshopper species and the cricket Acheta domesticus sequence as an outgroup (some data were purchased from the GeneBank Data Library (NCBI). In the phylogenetic tree, the Acridinae and Locustinae formed compact groups. Annexpected position of Celes scalozubovi (Locustinae) within the subfamily Acridinae indicated its vague phylogeny. The Catantopinae species lied close to the base of the Acridinae. Almost all branches of phylogenetic trees were strongly (55-100%) supported by bootstrap analysis.     

Antennal sensilla of grasshoppers (Orthoptera: Acrididae) in relation to food preferences and habits

The external structure, i.e. number and distribution of sensillae on male and female antennae of 12 species of grasshoppers belonging to Pamphaginae, Catantopinae, Oedipodinae and Gomphocerinae in the grasslands of Inner Mongolia was investigated using scanning electron microscopy. Five major types of antennal sensillae were detected - trichoid, long basiconic, short basiconic, slender and short basiconic, and coeloconic sensillae. Total number of antennal sensillae varied among different sexes, subfamilies, feeding groups, life forms and eco-forms. Males showed significantly more sensillae than females, due to presence of more short basiconic and coeloconic sensillae. Species under Catantopinae showed more long basiconic sensillae than the others. The Oedipodinae had the highest number of slender and short basiconic sensillae and coeloconic sensillae, followed by Catantopinae and Gomphocerinae; while Pamphaginae had the fewest. The total number of sensillae showed the same trend for these two types amongst the subfamilies as well, species which prefer habits on the ground possessed fewer antennal sensillae than species which prefer to stay on plants. The maximal number of antennal sensillae were observed in hygrophytous species,Chorthippus albomarginatus, in the 12 grasshopper species investigated, although the data is not statistically significant. The general trend which emerged was that species feeding on grass possessed more antennal sensillae, particularly coeloconic sensillae, compared to other feeding group species.     

The complete mitochondrial genome of Tonkinacris sinensis(Orthoptera: Acrididae): A tRNA-like sequence and its implications for phylogeny

The complete mitochondrial genome of Tonkinacris sinensis is 15,627 bp long and contains13 protein-coding genes (PCGs), 22 tRNA genes, 2 rRNA genes and one A + T-rich region. The gene order and orientation are identical to those of other Orthoptera species, containing the rearrangement of trnD and trnK. Intriguingly, a tRNA^Ser-like gene exists on the N strand between the trnSUCN and nad1 genes. The length of this gene is 110 bp, and it has a typical clover-leaf structure, an anticodon, and a high cove score (23.49). On its clover-leaf structure, on the anticodon arm, there is a 41 bp intron with an unknown function. Here, phylogenetic analysis was conducted based on 13 PCGs of 30 species from 9 subfamilies of Acrididae to understand their phylogenetic relationships. According to the phylogenetic tree, the relationship among the 9 subfamilies within Acrididae was as follows: (Spathosterninae + (Oxyinae + (Catantopinae + (Calliptaminae + (Cyrtacanthacridinae + (Melanoplinae + (Gomphocerinae + (Oedipodinae + Acridinae)))))))).     

Comparative mitogenome analysis of three species and monophyletic inference of Catantopinae (Orthoptera: Acridoidea)

To enrich the genomic database of Catantopinae (Orthoptera: Acrididae), mitogenomes of three species from different genera, Traulia nigritibialis (15,701 bp), Choroedocus capensis (16,293 bp) and Stenocatantops splendens (15,574 bp), were characterized and compared with those of other grasshoppers in the subfamily. All 13 protein-coding genes (PCGs) were initiated by ATN codons except COI with ACC (C. capensis and S.splendens) and ND6 with TTG (S. splendens). All transfer RNA (tRNA) genes had a typical clover-leaf structure, except tRNA^Ser(AGN) in which the base pairs of the dihydrouridine (DHU) arm were reduced. The phylogenetic relationships were constructed among 22 species from four subfamiles of Acrididae by classical classifications based on two datasets of their mitogenomes using both Bayesian Inference (BI) and Maximum Likelihood (ML). The phylogenetic analysis confirmed the monophyly of the three other subfamilies, but did not provided support of the monophyly of Catantopinae.     

Three new species of larval Charletonia Oudemans, 1910 (Acari: Prostigmata: Erythraeidae) and the first record of Charletonia krendowskyi (Feider, 1954) from Rhodes,Greece

Three new species of larval Charletonia Oudemans, 1910 from Rhodes, Greece are described: C. dalegori from an undetermined orthopteran, C. glifadaensis from Oedipoda sp. (Orthoptera: Acrididae: Oedipodinae) and C. kaliksti from Aiolopus sp. (Orthoptera: Acrididae: Oedipodinae). C. krendowskyi is recorded for the first time from Greece. A key to the European species of larval Charletonia is provided.     

不同起源时间的植物叶凋落物在中亚热带的分解特性

选择9种起源时间不同的植物的凋落叶,采用分解袋法,在浙江千岛湖地区从2006年6月到2008年6月进行了分解试验,试图探索植物进化过程中凋落物分解特性的演变趋势.所选的9种植物分属于4个类群,按起源时间由早到晚依次为蕨类植物(芒萁和桫椤)、裸子植物(苏铁、水杉、杉木和马尾松)、双子叶植物(木荷和青冈)及单子叶植物(毛竹).每隔一个月取样,每种凋落物3次重复.结果表明:不同植物类群凋落物基质的氮(N)、木质素(Lignin)含量及Lignin/N比值与分解速率具有良好的相关性.起源时间越晚的植物凋落物的基质N含量越高,为单子叶植物>双子叶植物>裸子植物>蕨类植物.Lignin含量和Lignin/N比值的趋势一致,均为起源时间越晚而值越低,即蕨类植物>裸子植物>双子叶植物>单子叶植物.凋落物分解系数k值的范围在0.25～0.63之间,表现出毛竹>青冈>木荷>水杉>马尾松>杉木>苏铁>桫椤>芒萁的趋势.4个植物类群的凋落物分解速率的均值为单子叶植物>双子叶植物>裸子植物>蕨类植物.试验结果初步表明:植物凋落物分解的进化趋势是由分解缓慢逐渐演变为分解较快.     

The phylogeny of Orthoptera inferred from mtDNA and description of Elimaea cheni （Tettigoniidae： Phaneropterinae） mitogenome

The complete 15,831 bp nucleotide sequence of the mitochondrial genome from Elimaea cheni(Phaneropterinae)was determined.The putative initiation codon for cox1 was TTA.The phylogeny of Orthoptera based on different mtDNA datasets were analyzed with maximum likelihood(ML)and Bayesian inference(BI).When all 37 genes(mtDNA)were analyzed simultaneously,the monophyly of Caelifera and Ensifera were recovered in the context of our taxon sampling.The phylogeny of Orthoptera was largely consistent with previous phylogenetie hypotheses.Rhaphidophoridae to be a sister group of Tettigoniidae,and the relationships among four subfamilies of Tettigoniidae were(Phaneropterinae+(Conocephalinae+(Bradyporinae+Tettigoniinae))).Pyrgomorphidae was the most basal group of Caelifera.The relationships among six acridid subfamilies were(Oedipodinae+(Acridinae+(Gomphocerinae+(Oxyinae+(Calliptaminae +Cyrtacanthaeridinae))))).However,we did not recover a monophyletic Grylloidea.Myrmecophilidae clustered into one clade with Gryllotalpidae instead of with Gryllidae.ML and BI analyses of all protein coding genes(using all nucleotide sequence data or excluding the third codon position,and amino acid sequences)revealed a topology identical to that of the entire mtDNA genome dataset.However,22 tRNAs genes excluding the DHU loop and T()C loop(TRNA),and two rRNA genes(RRNA)perform poorly when analyzed as single dataset.Our results suggest that the best phylogenetie inferences were ML and BI methods based on total mtDNA.Excluding tRNA genes,rRNA genes and the third codon position of protein coding genes from dataset and converting nucleotide sequences to amino acid sequences do not positively affect phylogenetic reconstruction.     

New insight into the evolution of aquaporins from flowering plants and vertebrates: orthologous identification and functional transfer is possible

Aquaporins (AQPs) represent a family of channel proteins that transport water and/or small solutes across cell membranes in the three domains of life. In all previous phylogenetic analysis of aquaporin, trees constructed using proteins with very low amino acid identity (<15%) were incongruent with rRNA data. In this work, restricting the evolutionary study of aquaporins to proteins with high amino acid identity (>25%), we showed congruence between AQPs and organismal trees. On the basis of this analysis, we defined 19 orthologous gene clusters in flowering plant species (3 PIP-like, 7 TIP-like, 6 NIP-like and 3 SIP-like). We described specific conserved motifs for each subfamily and each cluster, which were used to develop a method for automatic classification. Analysis of amino acid identity between orthologous monocotyledon and dicotyledon AQPs from each cluster, suggested that PIPs are under high evolutionary constraint. The phylogenetic analysis allowed us the assignment of orthologous aquaporins for very distant animal lineages (tetrapods-fishes). We also demonstrated that the location of all vertebrate AQPs in the ortholog clusters could be predicted by comparing their amino acid identity with human AQPs. We defined four AQP subfamilies in animals: AQP1-like, AQP8-like, AQP3-like and AQP11-like. Phylogenetic analysis showed that the four animal AQPs subfamilies are related with PIP-like, TIP-like, NIP-like and SIP-like subfamilies, respectively. Thus, this analysis would allow the prediction of individual AQPs function on the basis of orthologous genes from Arabidopsis thaliana and Homo sapiens.