欧亚大陆癞蝗科分类系统(直翅目:蝗亚目)

对分布于欧亚大陆的癞蝗科Pamphagidae昆虫进行了亚科分类研究,将已知的47个属分为6个亚科:锯癞蝗亚科Prionotropisinae nov.,蠢蝗亚科Thrinchinae,癞蝗亚科Pamphaginae,鸣癞蝗亚科Tropidaucheninae nov.,聋癞蝗亚科Nocarodesinae nov.,秃癞蝗亚科Orchaminae nov.,其中包括4个新亚科。建立了欧亚大陆癞蝗科新的分类系统。     

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Cytb基因序列探讨中国斑翅蝗科部分种类的系统发育关系

基于斑翅蝗科14种的线粒体Cytb基因462 bp序列,使用MEGA2和PAUP4.0b软件包进行分析,显示Cytb基因序列具有明显的高A、T偏向性和距离依赖的TS/TV值.采用邻接法(NJ)、最大似然法(MP)和极似然法(ML)分别构建斑翅蝗科4亚科8属的系统发育树,不同算法构建的系统发育树均支持分为四大分支(亚科):A(绿纹蝗属)、B(束颈蝗属)、C((飞蝗属+车蝗属)+小车蝗属)、D((痂蝗属+异痂蝗属)+皱膝蝗属);红胫小车蝗和黄胫小车蝗作为两个种比较合适;痂蝗亚科和异痂蝗亚科应该合并为一个亚科;飞蝗亚科与斑翅蝗亚科的分类关系尚未解决,需要进一步的研究进行分析验证.     

欧亚大陆裸蝗亚科的分类研究（直翅目: 蝗亚目: 蝗总科）

本文对欧亚大陆裸蝗亚科(Conophyminae)进行了系统的分类研究, 将其分为4个族, 其中包括3个新族, 即贝氏蝗族(Bienkoini tribe nov.)、庚蝗族（Genimenini tribe nov.）和普乐氏蝗族 （Plotnikovini tribe nov.）, 记述了一新属--原无翅蝗属Eozubovskya gen. nov., 并附已知4族25属的检索表。将该亚科中原有3个具翅的属（Khayyamia Kocak, 1981, Conophymacris Willemse, 1933 和Zagrosia Descamps, 1967）移出, 归入秃蝗亚科（Podisminae）。     

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。     

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。     

甘肃省痂蝗属一新种（蝗总科：斑翅蝗科）

本文记述采自甘肃省肃北县鱼儿红牧场的斑翅蝗科痂蝗属Ｂｒｙｏｄｅｍａ一新种,野马山痂蝗Ｂ．ｙｅｍａｓｈａｎａ ｓｐ．ｎｏｖ．,新种与透翅痂蝗Ｂ．ｈｙａｌｉｎａｌａ Ｚｈｅｎｇ ｅｔ Ｚｈａｎｇ近似。     

河北大学博物馆馆藏蝗总科的新属和新种(直翅目)

在整理河北大学博物馆馆藏的蝗总科标本中,发现1新属4新种,它们为斑腿蝗科Catantopidae的广西龙川蝗Longchuanacris guangxiensis sp.nov.,斑翅蝗科Oedipodidae的拟短腿蝗属Parahilethera gen.nov.,西藏拟短腿蝗Parahilethera xizangensis sp.nov.及淡黑纹束颈蝗Sphingonotus caerulistriatus sp.nov.,网翅蝗科Arcypteridae的拟中宽雏蝗Chorthippus parapricarius sp.nov..模式标本保存于河北大学博物馆.     

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。     

新疆斑翅蝗科三新种(直翅目,蝗总科)

记述分布在新疆地区斑翅蝗科Oedipodidae 3新种 ,即蓝胫胫刺蝗Compsorhipiscyanitibiasp .nov .,黑肛束颈蝗Sphingonotuspeliepiproctsp .nov .及托里束颈蝗Sphingonotustoliensissp .nov .,模式标本保存于陕西师范大学动物研究所标本室     

Systematics of Australian Thrasorinae (Hymenoptera, Cynipoidea, Figitidae) with descriptions of Mikeiinae, new subfamily, two new genera, and three new species

The Australian Thrasorinae are revised and Mikeius is transferred to Mikeiinae Paretas-Martínez & Pujade-Villar, subfam. n., and Mikeius clavatus Pujade-Villar & Restrepo-Ortiz, sp. n., is described. Two new genera of Thrasorinae are erected: Cicatrix Paretas-Martínez, gen. n., including Cicatrix pilosiscutum(Girault), comb. n. from Amblynotus, Cicatrix schauffi (Buffington), comb. n. from Mikeius, and Cicatrix neumannoides Paretas-Martínez & Restrepo-Ortiz, sp. n.; and Palmiriella Pujade-Villar & Paretas-Martínez, gen. n., including Palmiriella neumanni (Buffington), comb. n. from Mikeius, Thrasorus rieki Paretas-Martínez & Pujade-Villar, sp. n., is also described. A phylogenetic analysis of 176 morphological and biological characters, including all these new taxa and all genera previously included in Thrasorinae, was conducted. All subfamilies were recovered as monophyletic, with the following relationships: Parnipinae (Euceroptrinae (Mikeiinae (Plectocynipinae (Thrasorinae)))). A worldwide key to the subfamilies of Figitidae is provided that includes the new subfamily, as well as a key to genera Thrasorinae.     

The Neotropical ‘polymorphic earless praying mantises’ – Part I: molecular phylogeny and revised higher‐level systematics (Insecta: Mantodea,Acanthopoidea)

We perform phylogenetic analyses of the ‘polymorphic earless praying mantises’, a heterogeneous assemblage comprising c. 55% of mantodean diversity in the Neotropics. Bayesian and maximum‐likelihood were implemented on a DNA dataset of 9949 aligned nucleic acid characters comprising ten mitochondrial and nuclear genes. Our analyses largely resolved congruent relationships with high levels of support for higher‐level taxonomic groups, but revealed extensive inconsistencies between the resolved topology and morphology‐based classification systems. The polymorphic earless praying mantises, now granted superfamily status as the Acanthopoidea stat. n., comprises 8 families, 15 subfamilies and 18 tribes. Our newly revised organization required the following taxonomic changes: (i) Thespidae sensu n., including subfamilies Pseudopogonogastrinae subfam. n., Pseudomiopteryginae sensu n., Bantiinae subfam. n., Miobantiinae sensu n. and Thespinae sensu n. (tribes Musoniellini trib. n. and Thespini sensu n. ); (ii) Angelidae stat. n. et sensu n. ; (iii) Coptopterygidae stat. n. ; (iv) Liturgusidae sensu n. ; (v) Photinaidae stat. n., including Macromantinae stat. n., Cardiopterinae stat. n., Photiomantinae subfam. n. and Photinainae sensu n. (tribes Microphotinini trib. n., Orthoderellini stat. n. and Photinaini sensu n. ); (vi) Stenophyllidae stat. n. ; (vii) Acontistidae stat. n. ; and (viii) Acanthopidae sensu n. Our new system also resulted in the reassignment of various genera to new and existing higher‐level taxa, the exclusion of old world genera otherwise traditionally classified among the Thespidae, Liturgusidae and Angelidae, the confirmation of Stenophylla Westwood as member of this clade, and the revalidation of Paradiabantia Piza stat. r. We provide diagnoses for all suprageneric taxa using external morphological characters and male genitalia. A key to higher‐level groups is provided. We incorporate egg case structural variation as a novel approach for taxon delineation. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:29E37322‐30EB‐4F64‐80C9‐E2149B5B0195 .     

Phylogeny of the Cardiidae (Mollusca, Bivalvia): Protocardiinae, Laevicardiinae, Lahilliinae, Tulongocardiinae subfam. n. and Pleuriocardiinae subfam. n.

In a preliminary cladistic analysis of the bivalve family Cardiidae (Schneider 1992), members of the subfamilies Protocardiinae, Lahilliinae, and Laevicardiinae, plus the genus Nemocardium , were found to be the least derived taxa of cardiids. A cladistic analysis is undertaken of the genera and subgenera of these cardiid taxa, plus several Mesozoic taxa which have never been assigned to any subfamily. The Late Triassic Tulongocardium , which is placed in Tulongocardiinae subfam. n., is the sister taxon to all other cardiids. Protocardiinae is restricted to the genus Protocardia. Most other Mesozoic taxa which have been placed in the Protocardiinae are found to be members of the Lahilliinae. Nemocardium is placed in the Laevicardiinae. Incacardium, Pleuriocardia , and Dochmocardia form a monophyletic group, Pleuriocardiinae subfam. n. Pleuriocardiinae, Laevicardiinae, and the remaining members of the Cardiidae (herein informally termed "cucardiids") form a monophyletic group.     

Scomberomorocotyle munroi n. g., n. sp. (Scomberomorocotylinae n. subf.), a thoracocotylid monogenean from Scomberomorus munroi (Scombridae) off Australia and Papua New Guinea

Scomberomorocotyle munroi n. g., n. sp. is described from the gills of Scomberomorus munroi, a Spanish mackerel from the coasts of northern Australia and southern Papua New Guinea. The genus belongs to the suborder Gastrocotylinea because a pair of basal accessory sclerites is present in the clamps. However, the worm does not belong to any of the eight gastrocotylinean families as they are currently recognised. The worm appears to be a member of the Thoracocotylidae, in that the male copulatory organ has relatively weakly developed spines, and that the haptor is one-sided with two rows of clamps. However, the worm differs from all thoracocotylids in that the clamps lack the characteristic lateral rib-like thickenings. To accommodate the new genus and species, the diagnosis of the Thoracocotylidae Price is amended to include worms lacking ribs in their clamps, and a new subfamily, the Scomberomorocotylinae n. subfam., is erected; a key to the four subfamilies which we recognise as valid is provided.     

Myxinidocotyle gen.n. and Lophocotyle Braun (Platyhelminthes, Monogenea, Acanthocotylidae) with descriptions of three new species from hagfishes (Chordata, Myxinidae)

Three new species of monogencans parasitizing hagfish are described: Myxinidocotyle californica gen. et sp.n., M. japonica sp.n. and Lophocotyle novaezeelandica sp.n. The pseudohaptor of Myxinidocotyle has 8+8 transverse ridges that never attain the radial arrangement characterizing Lophocotyle and Acanthocotyle . There are no sclerites in the pseudohaptoral ridges of Myxinidocotyle and Lophocotyle . The male reproductive system of Myxinidocotyle and Lophocotyle differs from that of Acanthocotyle in having a bilateral accessory gland apparatus and an armed copulatory organ. The femrle reproductive system has a large vaginal receptaculum scminis; in Myxinidocotyle with two vagino-intestinal canals. The uterine pore and the male genital pore are close together and the vaginal pore is situated posterior to them, on the left ventral side of the body. We conclude that Myxinidocotyle, Lophocotyle and Acunrkocotyle represent different levels of acanthocotylid evolution. Myxinidocotyle being the most primitive. The family Acanthocotylidac is divided into the subfamilies Myxinidoeutylinae subfam.n., Lophocotylinae and Acanthoeutylinae.     

Evolution and systematics of the Late Paleozoic brachiopod family Linoproductidae with descriptions of species from the Lower Permian of the Northern Timan

The analysis of the morphological features of the genera of the family Linoproductidae in the Late Paleozoic substantiates its three subfamilies as three evolutionary trends beginning with the initial subfamily Coopericinae Lazarev, 2004, which is known from the beginning of the Early Carboniferous and two its derivatives: subfamily Linipalinae subfam. nov., which appeared in the Podolskian Time (Upper Moscovian Age), and subfamily Linoproductinae Stehli, 1954, which appeared in the Kasimovian Age. The problems and prospects of the further detailing of the system of these subfamilies are discussed. Three new species of the genus Sublinoproductus are described from the Lower Permian of Northern Timan.     

Taxonomie und Systematik der HippocardioideaPojeta & Runnegar, 1976 [n. superfam.] (Mollusca; Rostroconchia)

The revisions of the families PseudobigaleaidaeHoare, Mapes &; Yancey, 2002 and HippocardiidaePojeta &; Runnegar, 1976 led to the introduction of a new taxon at the superfamily rank in order to unite the two families and distinguish them from the members of the Conocardiidae and Bransoniidae within the order Conocardiida. The autapomorphy of this new superfamily HippocardioideaPojeta &; Runnegar, 1976 [n. superfam.] — the more or less uniform development of at least one hood — is considered taxonomically as so important that we exclude a common ancestry of the almost contemporaneously occurring taxa of the Hippocardiidae, Pseudobigaleaidae on the one hand and the Bransoniidae sensuPojeta &; Runnegar on the other. The family Hippocardiidae is divided into six taxa on subfamily rank, the HippocardiinaePojeta &; Runnegar, Babinicardiinae n. subfam., Barrandeicardiinae n. subfam., Bohemicardiinae n. subfam., Goticardiinae n. subfam. and Hassiacardiinae n. subfam. At the species level, 13 taxa are assigned to the generaBabinicardia n. gen.,Barrandeicardia n. gen.,Bohemicardia n. gen.,Filicardia n. gen,.Globocardia n. gen.,Goticardia n. gen.,Pohlia n. gen. andHassiacardia n. gen. Additionally, the speciesGoticardia kauffmannii n. gen. n. sp. is introduced, whereas the primary homonymy of ?Conocardium“reticulatum Babin, 1966 is retained, because this taxon remained inassignable to any of the existing genera, but is considered as a member of the Hippocardiidae. The revised family Hippocardiidae occurred stratigraphically from the Middle Silurian (Wenlockian) until Mississippian time; members of the new superfamily Hippocardioidea are known from the Ordovician until the Pennsylvanian.     

New subfamily Petschoricinae and its position in the system of Foraminifera

A new foraminiferal subfamily, Petschoricinae subfam. nov., with the type genus Petschorica Suchov, 2012, from the Ufimian (Upper Permian) of the Pechora Province is described. The subfamily belongs to the family Saccamminidae and differs from all other subfamilies of this family in the presence of small supplementary apertures, which are irregular in shape and scattering on the test surface. The family Saccamminidae is included in the order Saccamminida of the subclass Hormosinana Mikhalevich, 1992, class Nodosariata Mikhalevich, 1992.