巨噬细胞极化在类风湿关节炎中的作用

类风湿关节炎(rheumatiod arthritis,RA)是侵犯骨和关节为主的多系统炎症的自身免疫性疾病。巨噬细胞具有吞噬?趋化?免疫调节等功能,参与特异性和非特异性免疫应答,其在RA的发生发展中起到至关重要的作用。巨噬细胞不同亚型极化及其作用是近年来RA的致病机制的研究热点。巨噬细胞主要分为经典活化M1型和选择活化M2型。RA患者机体内免疫炎症反应直接影响外周血、滑膜和滑液巨噬细胞的极化,使M1型促炎性巨噬细胞不断增加,从而打破M1/M2平衡状态。现总结巨噬细胞的极化及其在RA发生发展中的作用?     

M2型巨噬细胞极化及相关疾病的研究进展

巨噬细胞是固有免疫的重要成员,在机体防御病原微生物感染、肿瘤、过敏性疾病、代谢类疾病、组织损伤修复等发生发展过程中发挥着极其重要的作用。在微环境,尤其是多种细胞因子的影响下,巨噬细胞极化成M1/M2型巨噬细胞,表达相应的特异性基因,行使不同的功能。M1型巨噬细胞主要发挥促炎、杀菌及呈递抗原的功能,M2型巨噬细胞主要起抑炎、抗寄生虫感染和组织修复的作用。现总结人们对巨噬细胞极化的认识过程、M2型巨噬细胞的分类和其形成过程中起重要调控作用的信号分子,并着重讨论M2型巨噬细胞在相关疾病中的功能。     

钙黏蛋白家族与巨噬细胞极化的关系

巨噬细胞参与固有免疫和适应性免疫过程,它有两种极化类型:经典激活型(M1型)和替代激活型(M2型)。在不同病理过程(如过敏性炎症、肿瘤迁移、免疫炎症等)的发生进程中,巨噬细胞均发挥着重要作用。钙黏蛋白是一种介导细胞识别和黏附作用的膜蛋白分子,近些年来有研究表明钙黏蛋白家族与巨噬细胞极化有着紧密的联系。现主要就E-钙黏蛋白、N-钙黏蛋白、VE-钙黏蛋白、OB-钙黏蛋白、T-钙黏蛋白与巨噬细胞极化的相互作用,以及它们在炎症反应中的作用和机制作一概述。     

MicroRNA调控小胶质细胞极化在神经系统疾病中的作用和机制研究进展

小胶质细胞是定居于中枢神经系统的巨噬细胞,其激活介导的免疫炎症反应在多种神经系统疾病的病理进程中均扮演极其重要的角色。激活的小胶质细胞存在M1和M2两种形态、功能显著不同的极化类型。M1型细胞主要发挥杀菌和促炎作用,M2型细胞则具有抗炎和促进神经修复等功能。越来越多的证据表明,micro RNA(mi RNA)在不同极化状态的小胶质细胞中表达模式存在明显差异,mi RNA可以调控小胶质细胞的极化过程,并进一步影响神经疾病的病理进展。充分阐明疾病发病过程中小胶质细胞的极化亚型及其mi RNA调节机制,有助于深入认识小胶质细胞参与神经系统疾病发病的免疫病理机制,为寻找更加有效的神经疾病治疗新靶点提供理论依据。     

巨噬细胞极化的研究进展

巨噬细胞是一群表型和功能均具有高度异质性的免疫细胞。巨噬细胞通过清除并修复受损的细胞和基质来维护组织完整性。巨噬细胞在不同的组织微环境、不同病理条件下,可极化成不同的表型即M1型巨噬细胞(经典活化的巨噬细胞)和M2型巨噬细胞(替代活化的巨噬细胞)。本文将对不同巨噬细胞亚群在抗细菌感染、抗寄生虫感染、哮喘、动脉粥样硬化和肿瘤产生中起到的的保护或致病作用,以及调控巨噬细胞极化的机制进行综述。掌握巨噬细胞极化在不同疾病中的作用以及调控巨噬细胞极化的具体机制,将为疾病的预防、诊断、治疗及药物研发提供新策略。     

巨噬细胞极化及其在慢性阻塞性肺疾病中的作用

巨噬细胞具有高度可塑性,在炎症因子的诱导和多种信息分子的调控下可极化为经典活化巨噬细胞(M1)和替代活化巨噬细胞(M2)。慢性肺部炎症反应和肺实质损伤是慢性阻塞性肺疾病(chronic obstructive pulmonary disease, COPD)的主要病理表现。M1促进肺部炎症反应;M2抑制炎症反应,参与肺组织损伤与修复,并吞噬和清除病原微生物和凋亡细胞。靶向干预巨噬细胞极化方向有可能成为COPD治疗的新策略。     

NLRP3炎性小体研究新进展

NLRP3炎性小体是一种分子量约为700Kda的大分子多蛋白复合体,能被多种病原相关的分子模式或损伤相关的分子模式活化,对固有免疫系统免疫功能的发挥具有极其重要的作用。但如果其被过度激活则可通过活化的半胱天冬酶-1持续地将pro-IL-1β和pro-IL-18剪切为成熟的IL-1β和IL-18,进而激活下游信号转导通路,产生大量的炎性介质,引起机体发生严重的炎症反应,最终促进多种炎症性疾病的发生与发展,如Muckle—wells综合征、2型糖尿病、非酒精性脂肪肝、动脉粥样硬化、炎症性肠病和阿尔兹海默病等。因此,对NLRP3炎性小体进行深入的研究不仅有助于阐释固有免疫系统如何有效地发挥其免疫功能,而且作为系列炎症反应的核心,NLRP3炎性小体：还可能成为多种炎症性疾病防治的新靶点。我们就NLRP3炎性小体的结构与功能,激活与调控,分布与疾病的近期研究作一综：违。     

病毒感染引起的炎症反应：宿主对抗病毒的“双刃剑”

先天性免疫系统作为宿主抵抗外来病原入侵的第一道防线,也是最迅速的防御系统。宿主先天性免疫系统中的模式识别受体识别入侵信号并激活炎症信号通路,诱导产生大量促炎性细胞因子,引起炎症反应。病毒感染是激活炎症反应的条件之一,诱导机体产生强烈的免疫应答,强大的炎症反应调控网络在宿主抗病毒过程中发挥关键作用,以维持机体的平衡。本文综述了病毒感染引起的炎症反应,重点介绍了宿主对炎症反应的调控网络,以及DNA和RNA病毒对炎症反应的调节机制,为病毒感染引起的免疫性疾病的治疗提供参考。     

NLRP3 炎性小体研究新进展

NLRP3 炎性小体是一种分子量约为700Kda 的大分子多蛋白复合体,能被多种病原相关的分子模式或损伤相关的分子模式 活化,对固有免疫系统免疫功能的发挥具有极其重要的作用。但如果其被过度激活则可通过活化的半胱天冬酶-1 持续地将 pro-IL-1茁和pro-IL-18 剪切为成熟的IL-1茁和IL-18,进而激活下游信号转导通路,产生大量的炎性介质,引起机体发生严重的炎 症反应,最终促进多种炎症性疾病的发生与发展,如Muckle-Wells综合征、2 型糖尿病、非酒精性脂肪肝、动脉粥样硬化、炎症性肠 病和阿尔兹海默病等。因此,对NLRP3 炎性小体进行深入的研究不仅有助于阐释固有免疫系统如何有效地发挥其免疫功能,而 且作为系列炎症反应的核心,NLRP3 炎性小体还可能成为多种炎症性疾病防治的新靶点。我们就NLRP3 炎性小体的结构与功 能,激活与调控,分布与疾病的近期研究作一综述。     

抗病毒免疫中干扰素与炎症信号通路的交互调控：防御反应与维持稳态

天然免疫是机体通过识别自身或外部危险信号后,为维持体内稳态而逐步建立起来的一系列防御反应,当宿主细胞内的模式识别受体识别胞内病原相关分子模式后激活干扰素(interferon, IFN)、核因子-kappa B (nuclear factor-kappa B, NF-κB)和炎性小体等信号通路。IFNs在天然免疫应答中发挥重要作用,它诱导的抗病毒基因能够通过多种方式抵御病毒的感染,炎症反应则是机体自动的防御反应,能够在病毒感染机体时释放促炎性细胞因子以调控机体的免疫反应,进而发挥抗病毒作用。在病毒感染过程中,IFN信号通路与炎症反应调控网络中的关键分子如NF-κB/RelA、PKR等存在一定的交互作用,此外,IFN信号通路及其产生的细胞因子又影响其他信号通路的活化,进而调控机体的免疫应答以维持自身稳态,它们之间的交互调控失衡将会引起过度炎症反应,导致组织器官的免疫病理损伤,例如SARS-CoV-2感染机体时产生的过度炎症反应。本文综述了机体抗病毒免疫过程中干扰素信号通路与炎症反应之间的交互调控,为研发抗病毒策略提供新思路。     

True bugs (Hemiptera,Heteroptera) as psyllid predators (Hemiptera,Psylloidea)

Data on natural enemies of psyllids are rare and can usually be found in papers about economically significant species. During an investigation of psyllid fauna in Serbia, natural enemies were investigated, too. True bugs were the most numerous among them. From 28 psyllid species, 21 species of true bugs from families Anthocoridae and Miridae were reared. Seven species of Anthocoridae were identified: Anthocoris amplicollis (Horváth, 1839), Anthocoris confusus Reuter, 1884, Anthocoris nemoralis (Fabricius, 1794), Anthocoris nemorum (Linnaeus, 1761), Orius majusculus Reuter, 1884, Orius minutus (Linnaeus, 1758) and Orius niger Wolff, 1811. The following 14 species of Miridae were identified: Atractotomus mali Meyer-Dür, 1843, Campylomma verbasci (Meyer-Dür, 1843), Deraeocoris flavilinea (A. Costa, 1862), Deraeocoris ruber (Linnaeus, 1758), Deraeocoris lutescens (Schilling, 1836), Heterocordylus genistae (Scopoli, 1763), Hypseloecus visci (Puton, 1888), Malacocoris chlorizans Panzer, 1794, Miris striatus (Linnaeus, 1758), Orthotylus marginalis Reuter, 1884, Psallus assimilis Stichel, 1956, Psallus quercus Kirschbaum, 1856, Psallus flavellus Stichel, 1933 and Pseudoloxops coccinea (Meyer-Dür, 1843). The aim of the research was to provide list of true bugs recorded as predators of psyllids in order to preserve their diversity and significance, especially on cultivated plants.     

Review of the sawfly genus Empria (Hymenoptera, Tenthredinidae) in Japan

The following eleven Empria species are reported from Japan: Empria candidata (Fallén, 1808), Empria japonica Heidemaa & Prous, 2011, Empria liturata (Gmelin, 1790), Empria loktini Ermolenko, 1971, Empria plana (Jakowlew, 1891), Empria quadrimaculata Takeuchi, 1952, Empria rubicola Ermolenko, 1971, Empria tridens (Konow, 1896), Empria tridentis Lee & Ryu, 1996, Empria honshuana Prous & Heidemaa, sp. n., and Empria takeuchii Prous & Heidemaa, sp. n. The lectotypes of Poecilosoma pallipes Matsumura, 1912, Empria itelmena Malaise, 1931, Tenthredo candidata Fallén, 1808, and Tenthredo (Poecilostoma) hybrida Erichson, 1851 are designated. Empria itelmena Malaise, 1931, syn. n. is synonymized with Empria plana (Jakowlew, 1891). Poecilosoma pallipes Matsumura, 1912, previously assigned to Empria, is transferred to Monsoma, creating Monsoma pallipes (Matsumura, 1912), comb. n. Results of phylogenetic analyses using mitochondrial (COI) and nuclear (ITS1 and ITS2) sequences are also provided.     

New systematic assignments in Gonyleptoidea (Arachnida, Opiliones, Laniatores)

As part of an ongoing revision of the family Gonyleptidae, we have identified many species that are synonyms of previously described species or misplaced in this family. This article summarizes these findings, adding previously unavailable information or correcting imprecise observations to justify the presented taxonomic changes. The following new familial or subfamilial assignments are proposed: Nemastygnus Roewer, 1929 and Taulisa Roewer, 1956 are transferred to Agoristenidae, Agoristeninae; Napostygnus Roewer, 1929 to Cranaidae; Ceropachylinus peruvianus Roewer, 1956 and Pirunipygus Roewer, 1936 are transferred to Gonyleptidae, Ampycinae; Gyndesops Roewer, 1943, Haversia Roewer, 1913 and Oxapampeus Roewer, 1963 are transferred to Gonyleptidae, Pachylinae. The following generic synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes Mello-Leitão, 1922 = Centroleptes Roewer, 1943; Acrographinotus Roewer, 1929 = Unduavius Roewer, 1929; Gonyleptes Kirby, 1819 = Collonychium Bertkau, 1880; Mischonyx Bertkau, 1880 = Eugonyleptes Roewer, 1913 and Gonazula Roewer, 1930; Parampheres Roewer, 1913 = Metapachyloides Roewer, 1917; Pseudopucrolia Roewer, 1912 = Meteusarcus Roewer, 1913; Haversia Roewer, 1913 = Hoggellula Roewer, 1930. The following specific synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes singularis (Mello-Leitão, 1935) = Centroleptes flavus Roewer, 1943, syn. n.; Geraeocormobius sylvarum Holmberg, 1887 = Discocyrtus serrifemur Roewer, 1943, syn. n.; Gonyleptellus bimaculatus (Sørensen, 1884) = Gonyleptes cancellatus Roewer,1917, syn. n.; Gonyleptes atrus Mello-Leitão, 1923 = Weyhia brieni Giltay, 1928, syn. n.; Gonyleptes fragilis Mello-Leitão, 1923 = Gonyleptes banana Kury, 2003, syn. n.; Gonyleptes horridus Kirby, 1819 = Collonychium bicuspidatum Bertkau, 1880, syn. n., Gonyleptes borgmeyeri Mello-Leitão, 1932, syn. n., Gonyleptes curvicornis Mello-Leitão, 1932, syn. n., Metagonyleptes hamatus Roewer, 1913, syn. n. and Paragonyleptes simoni Roewer, 1930, syn. n.; Gonyleptes pustulatus Sørensen, 1884 = Gonyleptes guttatus Roewer, 1917, syn. n.; Haversia defensa (Butler, 1876) = Sadocus vallentini Hogg, 1913, syn. n.; Liogonyleptoides minensis (Piza, 1946) = Currala bahiensis Soares, 1972, syn. n.; Megapachylus grandis Roewer, 1913 = Metapachyloides almeidai Soares & Soares, 1946, syn. n.; Mischonyx cuspidatus (Roewer, 1913) = Gonazula gibbosa Roewer, 1930 syn. n.; Mischonyx scaber (Kirby, 1819) = Xundarava holacantha Mello-Leitão, 1927, syn. n.; Parampheres tibialis Roewer, 1917 = Metapachyloides rugosus Roewer, 1917, syn. n.; Parapachyloides uncinatus (Sørensen, 1879) = Goyazella armata Mello-Leitão, 1931, syn. n.; Pseudopucrolia mutica (Perty, 1833) = Meteusarcus armatus Roewer, 1913, syn. n. The following new combinations are proposed: Acrographinotus ornatus (Roewer, 1929), comb. n. (ex Unduavius); Gonyleptellus bimaculatus (Sørensen, 1884),comb. n. (ex Gonyleptes);Gonyleptes perlatus (Mello-Leitão, 1935), comb. n. (exMoojenia);Mischonyx scaber (Kirby, 1819), comb. n. (ex Gonyleptes); and Neopachyloides peruvianus (Roewer, 1956), comb. n. (ex Ceropachylus). The following species of Gonyleptidae, Gonyleptinae are revalidated: Gonyleptes atrus Mello-Leitão, 1923 and Gonyleptes curvicornis (Roewer, 1913).     

Annotated type catalogue of the Orthalicoidea (Mollusca,Gastropoda) in the Museum für Naturkunde,Berlin

The type status is described of 96 taxa classified within the superfamily Orthalicoidea and present in the Mollusca collection of the Museum für Naturkunde der Humboldt-Universität zu Berlin. Lectotypes are designated for the following taxa: Orthalicus elegans Rolle, 1895; Bulimus maranhonensis Albers, 1854; Orthalicus nobilis Rolle, 1895; Orthalichus tricinctus Martens, 1893. Orthalicus sphinx tresmariae is introduced as new name for Zebra sphinx turrita Strebel, 1909, not Zebra quagga turrita Strebel, 1909. The following synonyms are established: Zebra crosseifischeri Strebel, 1909 = Orthalicus princeps fischeri Martens, 1893; Orthalicus isabellinus Martens, 1873 = Orthalicus bensoni (Reeve, 1849); Zebra zoniferus naesiotes Strebel, 1909 = Orthalicus undatus (Bruguière, 1789); Porphyrobaphe (Myiorthalicus) dennisoni pallida Strebel, 1909 = Hemibulimus dennisoni (Reeve, 1848); Zebra delphinus pumilio Strebel, 1909 = Orthalicus delphinus (Strebel, 1909); Orthalicus (Laeorthalicus) reginaeformis Strebel, 1909 = Corona perversa (Swainson, 1821); Bulimus (Eurytus) corticosus Sowerby III, 1895 = Plekocheilus (Eurytus) stuebeli Martens, 1885. The taxon Bulimus (Eudioptus) psidii Martens, 1877 is now placed within the family Sagdidae, tentatively in the genus Platysuccinea. Appendices are included with an index to all the types of Orthalicoidea extant (including those listed by Köhler 2007) and a partial list of letters present in the correspondence archives.     

New genera,species and records of Phaneropterinae (Orthoptera,Phaneropteridae) from sub-Saharan Africa

The results of the study of many specimens preserved in different European museums are reported. The tribe Terpnistrini Brunner von Wattenwyl, 1878 is resurrected. The distribution of the following species is enhanced: Pardalota asymmetrica Karsch, 1896, Diogena denticulata Chopard, 1954, Diogena fausta (Burmeister, 1838), Plangiopsis adeps Karsch, 1896, Poreuomena sanghensis Massa, 2013 and Tylopsis continua (Walker, 1869). Further, for their peculiar characteristics, two African representatives of the American genus Symmetropleura Brunner von Wattenwyl, 1878 are included in two new genera: Symmetrokarschia africana (Brunner von Wattenwyl, 1878), comb. n. and Symmetroraggea dirempta (Karsch, 1889), comb. n. A new genus and species from the Democratic Republic of Congo, Angustithorax spiniger gen. n., sp. n., and a new genus and species from Tanzania, Arostratum oblitum gen. n., sp. n. are described. Finally Melidia claudiae sp. n. and Atlasacris brevipennis sp. n. are described and compared with related species.     

Systematics of the parasitic wasp genus Oxyscelio Kieffer (Hymenoptera,Platygastridae s.l.), part II: the?Australian and southwest Pacific fauna

The Australasian and southwest Pacific species of Oxyscelio (Hymenoptera: Platygastridae s.l.) are revised. A total of 80 species are recognized as valid, 13 of which are redescribed: O. atricoxa (Dodd), O. concoloripes (Dodd), O. flavipes (Kieffer), O. grandis (Dodd), O. hyalinipennis (Dodd), O. magniclava (Dodd), O. mirellus (Dodd), O. montanus (Dodd), O. nigriclava (Dodd), O. nigricoxa (Dodd), O. rugulosus (Dodd), O. shakespearei (Girault), and O. solitarius (Dodd). Oxyscelio glabriscutellum (Dodd) syn. n. is placed as a subjective junior synonym of O. rugulosus. Sixty-seven new species are described, many representing new distributional records for the genus - O. aciculae Burks, sp. n., O. anfractus Burks, sp. n., O. bellariorum Burks, sp. n., O. bicoloripedis Burks, sp. n., O. brevitas Burks, sp. n., O. catenae Burks, sp. n., O. caudarum Burks, sp. n., O. circulorum Burks, sp. n., O. clivi Burks, sp. n., O. clupei Burks, sp. n., O. conjuncti Burks, sp. n., O. contusionis Burks, sp. n., O. corrugationis Burks, sp. n., O. croci Burks, sp. n., O. cuspidis Burks, sp. n., O. densitatis Burks, sp. n., O. dissimulationis Burks, sp. n., O. divisionis Burks, sp. n., O. exiguitatis Burks, sp. n., O. fluctuum Burks, sp. n., O. foliorum Burks, sp. n., O. funis Burks, sp. n., O. gressus Burks, sp. n., O. hamorum Burks, sp. n., O. incisurae Burks, sp. n., O. lenitatis Burks, sp. n., O. leviventris Burks, sp. n., O. limbi Burks, sp. n., O. liminis Burks, sp. n., O. linguae Burks, sp. n., O. lintris Burks, sp. n., O. livens Burks, sp. n., O. mystacis Burks, sp. n., O. nasi Burks, sp. n., O. nitoris Burks, sp. n., O. obliquiatis Burks, sp. n., O. oblongiclypei Burks, sp. n., O. obturationis Burks, sp. n., O. oculi Burks, sp. n., O. palati Burks, sp. n., O. pectinis Burks, sp. n., O. pollicis Burks, sp. n., O. proceritatis Burks, sp. n., O. productionis Burks, sp. n., O. radii Burks, sp. n., O. rami Burks, sp. n., O. rupturae Burks, sp. n., O. sarcinae Burks, sp. n., O. scismatis Burks, sp. n., O. sciuri Burks, sp. n., O. scutorum Burks, sp. n., O. sepisessor Burks, sp. n., O. sinuationis Burks, sp. n., O. sordes Burks, sp. n., O. spatula Burks, sp. n., O. stipulae Burks, sp. n., O. stringerae Burks, sp. n., O. tenuitatis Burks, sp. n., O. truncationis Burks, sp. n., O. tubi Burks, sp. n., O. umbonis Burks, sp. n., O. uncinorum Burks, sp. n., O. valdecatenae Burks, sp. n., O. velamenti Burks, sp. n., O. verrucae Burks, sp. n., O. viator Burks, sp. n., and O. wa Burks, sp. n. The fauna is divided into nine diagnostic species groups, with five species unplaced to group.     

Sabellid and serpulid worm tubes (Polychaeta,Canalipalpata, Sabellida) from the historical stratotype of the Cenomanian (Late Cretaceous; Le Mans region,Sarthe, France)

The rich Cenomanian assemblage of tube-dwelling polychaete worms of the families Sabellidae and Serpulidae from Le Mans region (Sarthe) is described in detail for the first time in one place; the systematics and the palaeoecology of the species are discussed. The 19 species described belong to 12 genera: Glomerula Brünnich Nielsen, 1931; Filograna Berkeley, 1835; Protula Risso, 1826; Filogranula Langerhans, 1884; Serpula Linnaeus, 1758; Cementula Brünnich Nielsen, 1931; Neovermilia Day, 1961; Dorsoserpula Parsch, 1956; Mucroserpula Regenhardt, 1961; Placostegus Philippi, 1844; Cycloplacostegus Jäger, 2005; Pyrgopolon de Montfort, 1808. Two new species are described: Serpula? pseudoserpentina sp. nov. and Pyrgopolon (Septenaria) cenomanensis sp. nov.     

Revision,cladistic analysis and biogeography of Typhochlaena C. L. Koch, 1850, Pachistopelma Pocock, 1901 and Iridopelma Pocock, 1901 (Araneae,?Theraphosidae,Aviculariinae)

Three aviculariine genera endemic to Brazil are revised. Typhochlaena C. L. Koch, 1850 is resurrected, including five species; Pachistopelma Pocock, 1901 includes two species; and Iridopelma Pocock, 1901, six species. Nine species are newly described: Typhochlaena amma sp. n., Typhochlaena costae sp. n., Typhochlaena curumim sp. n., Typhochlaena paschoali sp. n., Pachistopelma bromelicola sp. n., Iridopelma katiae sp. n., Iridopelma marcoi sp. n., Iridopelma oliveirai sp. n. and Iridopelma vanini sp. n. Three new synonymies are established: Avicularia pulchra Mello-Leitão, 1933 and Avicularia recifiensis Struchen & Brändle, 1996 are junior synonyms of Pachistopelma rufonigrum Pocock, 1901 syn. n., and Avicularia palmicola Mello-Leitão, 1945 is a junior synonym of Iridopelma hirsutum Pocock, 1901 syn. n. Pachistopelma concolor Caporiacco, 1947 is transferred to Tapinauchenius Ausserer, 1871, making the new combination Tapinauchenius concolor (Caporiacco, 1947) comb. n. Lectotypes are newly designed for Pachistopelma rufonigrum Pocock, 1901 , Iridopelma hirsutum Pocock, 1901 and Pachistopelma concolor Caporiacco, 1947. Cladistic analyses using both equal and implied weights were carried out with a matrix comprising 62 characters and 38 terminal taxa. The chosen cladogram found with X-Pee-Wee and concavity 6 suggests they are monophyletic. All species are keyed and mapped and information on species habitat and area cladograms are presented. Discussion on biogeography and conservation is provided.     

A review of selected South- and East Asian Tanytarsus v.d. Wulp (Diptera: Chironomidae)

Male and pupa of Tanytarsus calorifontis sp. n. are described. Diagnoses, hypopygium drawings for the examined species and distribution are given for: Tanytarsus akantertiusSasa & Kamimura, T. angulatus Kawai, T. atagoensis Tokunaga,T. bathophilusKieffer, T. boninensis Tokunaga, T. formosae (Kieffer), T. formosanusKieffer, T. infundibulusChaudhuri & Datta, T. kikuchiiSasa, Kawai & Ueno, T. konishii Sasa & Kawai, T. mcmillani Freeman, T. mendax Kieffer, T. miyakobrevis Sasa & Hasegawa, T. monstrosus Chaudhuri et al., T. ogasaquartus Sasa & Suzuki, T. ogasatertius Sasa & Suzuki, T. okuboi Sasa & Kikuchi, T. oscillans Johannsen, T. ovatus Johannsen, T. oyamai Sasa, T. pollexus Chaudhuri & Datta, T. shouautumnalis Sasa, T. shoudigitatus Sasa, T. takahashii Kawai & Sasa, T. tamaundecimus Sasa, T. tonebeceus Sasa & Tanaka, T. tusimatneousSasa & Suzuki, T. unagiseptimus Sasa, T. uraiensis Tokunaga, T. yakuheiusSasa & Suzuki and T. yunosecundus Sasa. Tanytarsus ikiefeus Sasa & Suzuki is a new junior synonym of T. konishii. Tanytarsus ikifegeus Sasa & Suzuki, T. miyakoflavus Sasa & Hasegawa,T. oyabepallidus Sasa, Kawai & Ueno, T. simantoopeus Sasa et al. and T. tusimatheius Sasa & Suzuki are new junior synonyms of T. okuboi. Tanytarsus nippogregarius Sasa & Kamimura is a new junior synonym of T. bathophilus. Tanytarsus cultellus Chaudhuri & Datta and T. sibafegeus Sasa et al. are new junior synonyms of T. oscillans.Tanytarsus insulus (Guha et al., 1985) is a new junior synonym of T. ovatus. Tanytarsus sakishimanus Sasa & Hasegawa, T. vinculus Chaudhuri et al., T. parvistylus Chaudhuri & Datta, T. fusciabdominalis Guha et al. and T. euformosanus Kikuchi & Sasa are new junior synonyms of T. formosanus. Tanytarsus tsutaprimus Sasa, T. tokarajekeus Sasa & Suzuki, T. tusimatlemeus Sasa & Suzuki, T. tusimatopeus Sasa & Suzuki and T. yakugeheuus Sasa & Suzuki are new junior synonyms of T. shouautumnalis. Tanytarsus togasiroidus Sasa & Okazawa is a new junior synonym of T. shoudigitatus. Tanytarsus tusimatjekeus Sasa & Suzuki and T. tusimatkeleus Sasa & Suzuki are new junior synonyms of T. akantertius, and Tanytarsus tusimatpequeus Sasa & Suzuki is a new junior synonym of T. tusimatneous. Virgatanytarsus toganiveus (Sasa & Okazawa), Cladotanytarsus utonaiquartus (Sasa) and Zavrelia tusimatijeus (Sasa & Suzuki), all previously placed in Tanytarsus, are new combinations.