具尾蓝隐藻(Chroomonas caudata Geitler)研究──Ⅱ.藻蓝蛋白(Phycocyanin)的初步分析

初步分析了具尾蓝隐藻（ChroomonascaudataGeitler）的藻蓝蛋白,其吸收光谱为一双峰曲线,两个吸收峰分别为590nm和640nm。按A．N．Glazer等关于隐藻藻蓝蛋白分型的意见,具尾蓝隐藻的藻蓝蛋白属于Ⅱ型PC－645。     

具尾蓝隐藻(Chroomonas caudata Geitler)研究──Ⅱ.藻蓝蛋白(Phycocyanin)的初步分析

初步分析了具尾蓝隐藻的藻蓝蛋白,其吸收光谱为一双峰曲线,两个吸收峰分别为５９０ｎｍ放６４０ｎｍ,按Ａ．Ｎ．Ｇｌａｚｅｒ等关于隐藻藻蓝蛋白分型的意见具尾蓝隐菏的藻蓝蛋白属于Ⅱ型ＰＣ－６４５。     

柳树叶浸提液对四尾栅藻生长特性及光合效率的影响

以四尾栅藻（Scenedesmusquadncauda）为研究对象,应用柳树（sn如babylonica）叶浸提液研究了其对四尾栅藻密度、细胞形态、叶绿素含量及光合效率的影响。结果表明：各浓度柳树叶浸提液处理组四尾栅藻密度均低于对照组,且较高浓度浸提液处理组藻密度更低。浓度为10g／L、20g／L和30g／L的柳树叶浸提液对四尾栅藻的最大抑制率分别为47．0％、54．6％和62．3％。根据浓度一效应关系方程,计算出对应的柳叶浸提液96h对四尾栅藻的半效应浓度（EC,。值）为23．32g/L.加入柳树叶浸提液后,四尾栅藻细胞边缘变得不规则,细胞体变透明,部分细胞溶解。在柳树叶浸提液作用下四尾栅藻叶绿素a含量始终保持在很低的水平。lO∥L、20∥L和30∥L处理组叶绿素含量最低分别为173．12t,g／L、124．18斗∥L、37．62斗g／L。实验开始第ld后各浓度柳树叶浸提液处理组Fv／Fm显著下降（P〈0．01）,第24d柳树浸提液浓度效应较为明显,大致是浸提液浓度越高,四尾栅藻PSⅡ最大光合效率越低。     

汉中地区汉水流域水生维管植物种类及地理分布

经野外调查,采集标本与鉴定分析,汉中地区汉水流域共有水生维管植物69种,包括蕨类植物3种,种子植物66种,分别隶属于32科48属。其中挺水植物41种,浮水及浮叶植物11种,沉水植物17种。66种种子植物分别隶属于46属,有7种地理分布类型,其中以世界分布类型成分居多,共21属,占本地区水生种子植物总属数的45．7％;热带分布类型成分13属,占28．3％,温带分布类型12属,占26．0％。调查分析发现8种6该区域的新分布种,即：竹叶眼子菜,南方眼子菜,小茨藻,大茨藻,水毛花,穗花狐尾藻,有梗石龙尾的狸藻;新记录属4个,即：茨藻属,狐尾藻属,石龙尾属和狸藻属;新记录科2个,即;茨藻科和小二仙草科。     

穗状狐尾藻与不同生长期苦草种间竞争研究

水生植物之间的竞争作用在水体生态系统恢复过程中具有重要作用。本研究采用取代系列实验方法,对穗状狐尾藻(Myriophyllum spicatum L.)与不同生长期(幼苗期和成株期)苦草(Vallisneria natans(Lour.)Hara)的种间竞争进行了研究。结果显示,对于不同生长期的苦草,穗状狐尾藻均具有较强的竞争优势,成株期苦草的竞争能力强于其幼苗期;苦草成株组中的穗状狐尾藻平均株高比苦草幼苗组中的穗状狐尾藻平均株高增加了128.6%(P0.05),但苦草成株组中的穗状狐尾藻植株平均干重比苦草幼苗组中的穗状狐尾藻植株平均干重降低了62.8%(P0.05);苦草幼苗组中的穗状狐尾藻分枝较多、株丛大,对苦草幼苗形成了较大的遮光作用;苦草成株组中的穗状狐尾藻分枝少、植株较长,顶端漂浮于水面生长,表明受苦草的种间竞争压力增大,但仍小于穗状狐尾藻的种内竞争;另外,苦草幼苗组中的苦草根长比苦草成株组中的苦草根长平均长28.6%(P0.05),表明在与穗状狐尾藻竞争过程中,苦草幼苗更趋于竞争地下资源。本研究结果说明穗状狐尾藻竞争能力强于苦草,苦草幼苗受穗状狐尾藻的竞争影响较大。     

鼠尾藻生长与生殖的权衡

2009年7月初至2009年9月中旬对烟台长岛县望福礁附近水域鼠尾藻(Sargassum thunbergii)进行了生态学调查。实验设立固定采样地点通过随机采样以及现场标记测量的方法观测了鼠尾藻的生长与生殖情况。结果表明:(1)鼠尾藻生殖始于7月初,8月初为高峰期,此间87%的藻体产生生殖托;(2)藻体长度对成熟比例和生殖力均有显著的影响,藻体成熟具有大小依赖性;(3)营养组织生物量大的鼠尾藻群体生殖组织生物量也相对较大,生殖期间营养组织生长和生殖组织生长呈异速关系;(4)成熟藻体在有性生殖高峰期过后,生长率下降,而始终未成熟的藻体则持续生长(生长率0)。以上结果表明,在鼠尾藻的生活史中存在着生长与生殖的权衡。     

具尾蓝隐藻(Chroomonas caudata Geitler)研究──Ⅱ.藻蓝蛋白(Phycocyanin)的初步分析

初步分析了具尾蓝隐藻(Chroomonas caudata Geitler)的藻蓝蛋白,其吸收光谱为一双峰曲线,两个吸收峰分别为590nm和640nm。按A.N.Glazer等关于隐藻藻蓝蛋白分型的意见,具尾蓝隐藻的藻蓝蛋白属于Ⅱ型PC－645。     

武汉东湖隐藻门植物的分类学研究

隐藻门植物在各种淡水水体中很常见,其中卵形隐藻、啮蚀隐藻在国内被多次报道过。但是由于缺乏分类学的资料,国内关于隐藻门植物的报告并不完全准确,其类群也常常被忽视。我们在2009年6月到2010年3月间,不定期从武汉东湖的各个区域采集水样,共鉴定隐藻门植物4属8种：卵形隐藻、啮蚀隐藻、蛋白核隐藻、四蛋白核隐藻、马索隐藻、反曲弯隐藻、犀角织隐藻、具尾逗隐藻。其中四蛋白核隐藻和犀角织隐藻为中国新记录。作为具尾逗隐藻的异名,尖尾蓝隐藻此前也曾在国内被报道。     

沉水植物穗花狐尾藻耐盐性与生长

通过室内人工海水培养和杭州湾栽培实验,探究了穗花狐尾藻的耐盐能力及在低盐度水域中的生长情况。室内培养表明:穗花狐尾藻断枝可在盐度12以内的人工海水中正常生长;低盐度处理可促进不定根的生长;水体盐度达到15后,穗花狐尾藻叶绿素含量和最大光合效率Fv/Fm降低,生长停滞,大部分植株逐渐死亡。野外栽培表明:从2017年6月到2018年5月,穗花狐尾藻可在杭州湾水体盐度6.06～9.03,水温3.85～33.37℃条件存活,8—10月是穗花狐尾藻的快速生长期;穗花狐尾藻在杭州湾低盐度水体中可进行有性繁殖和无性繁殖,以无性繁殖为主。研究结果为穗花狐尾藻在低盐度水体中建立种群提供了依据。     

洪湖5种优势沉水植物光合荧光特性比较研究

利用水下饱和脉冲荧光仪(DIVING-PAM),原位观测洪湖5种优势沉水植物——苦草[Vallisneria natans(Lour.)Hara]、黑藻[Hydrilla verticillata(L.f.)Royle]、狐尾藻(Myriophyllum verticillatum L.)、菹草(Potamogeton crispus L.)和马来眼子菜(Potamogeton wrightii Morong)的量子产量及快速光曲线。结果显示:5种沉水植物苦草、黑藻、狐尾藻、菹草和马来眼子菜最大量子产量(Fv/Fm)分别为0.603、0.723、0.751、0.778和0.646。各物种的开放PSⅡ反应中心原初光能捕获效率(Fv′/Fm′)的大小依次为菹草狐尾藻黑藻马来眼子菜苦草,且除黑藻与狐尾藻间差异不显著外,其他物种间差异均显著;各物种光能利用能力(α)的大小依次为菹草黑藻狐尾藻马来眼子菜苦草,且除黑藻与狐尾藻间差异不显著外,其他物种间差异均显著;各物种无光抑制的最大潜在相对电子传递速率(rETRm)的大小依次为菹草狐尾藻黑藻马来眼子菜苦草,且各物种间差异显著;半饱和光强(Ek)的大小依次为狐尾藻菹草黑藻苦草马来眼子菜,且除狐尾藻与菹草间差异不显著外,其他物种间差异均显著。研究表明:洪湖5种优势沉水植物中,菹草和狐尾藻较耐强光,光合速率较高,而苦草则有较强的耐弱光能力。     

Comparative morphology of the carpel in the Liliaceae: Hewardieae, Petrosavieae, and Tricyrteae

The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.     

为《Flora of China》提供的伞形科新资料

在为编写《Flora of China》伞形科而进行的修订工作中,提出了11个新组合,即矮小丝瓣芹Acronema minus (M. F. Watson) M. F. Watson & Z. H. Pan, 短柄丝瓣芹A. brevipedicellatum Z. H. Pan & M. F. Watson, 川西当归Angelica sinensis var. wilsonii (H. Wolff) Z. H. Pan & M. F. Watson, 云南细裂芹Harrysmithia franchetii (M. Hiroe) M. L. Sheh, 钝叶独活Heracleum candicans var. obtusifolium (Wall. ex DC.) F. T. Pu & M. F. Watson, 中华天胡荽Hydrocotyle hookeri ssp. chinensis (Dunn ex R. H. Shan & S. L. Liou) M. F. Watson & M. L. Sheh, 普渡天胡荽H. hookeri ssp. handelii (H. Wolff) M. F. Watson & M. L. Sheh, 锐棱岩风Libanotis grubovii (V. M. Vinogradova) M. L. Sheh & M. F. Watson, 美脉藁本Ligusticum likiangense (H. Wolff) F. T. Pu & M. F. Watson和线叶藁本L. nematophyllum (Pimenov & Kljuykov) F. T. Pu & M. F. Watson, 无管藁本L. nullivittatum (K. T. Fu) F. T. Pu & M. F. Watson和二色棱子芹Pleurospermum bicolor (Franch.) C. Norman ex Z. H. Pan & M. F. Watson.; 发现了1个新种,即短柄丝瓣芹。此外,还为Pleurospermum govanianum var. bicolor Franch.指定了后选模式。     

Entomopathogenic Nematode Infectivity Assay: Comparison of Penetration Rate into Different Hosts

Penetration rate (the percentage of the initial infective juvenile inoculum that invades an insect host) was tested as an indicator of entomopathogenic nematode infectivity. Several host-parasite-substrate combinations were evaluated for penetration rate. Four steinernematids, Steinernema carpocapsae, S. glaseri, S. feltiae, S. riobravis and two strains of Heterorhabditis bacteriophora were tested in a contact bioassay against the wax moth, Galleria mellonella, the yellow meal worm, Tenebrio molitor, the beet armyworm, Spodoptera exigua, the black cutworm, Agrotis ipsilon, and the European corn borer, Ostrinia nubilalis. The insect larvae were confined individually in sand and filter paper arenas and exposed to 200 infective juveniles. After incubation, dead insects were dissected in order to count the nematodes penetrated. The data were analyzed for the effects of nematode strain and substrate on penetration rate. The bioassay substrate had a variable effect depending on the insect species. The nematode effect was highly significant for all insects tested. The penetration rate therefore allowed comparisons among nematode strains invading a host. Nematode ranking for infectivity differed according to the insect tested.     

Enterovirus 71 3C proteolytically processes the histone H3 N-terminal tail during infection

Highlights
1. The N-terminal tail of histone H3 is specifically cleaved during EV71 infection.
2. Viral protease 3C is identified as a protease responsible for proteolytically processing the N-terminal H3 tail.
3. Our finding reveals a new epigenetic regulatory mechanism for Enterovirus 71 in virus-host interactions.     

The Role of Parasitoids and Entomopathogenic Fungi in Mortality of Third-instar and Adult Ceroplastes destructor and C. sinensis (Hemiptera: Coccidae: Ceroplastinae) on Citrus in New Zealand

The incidence of parasitism and disease in third-instar and adult Ceroplastes destructor Newstead and C. sinensis Del Guercio (Hemiptera: Coccidae) on citrus in Northland, New Zealand, was measured from 1991-1994. Both species were parasitized by female Euxanthellus philippiae Silvestri (Hymenoptera: Aphelinidae). Female E. philippiae were hyper-parasitized by males of their own species and by Coccidoctonus dubius Girault (Hymenoptera: Encyrtidae). Male E. philippiae were also tertiary parasitoids of C. dubius. E. philippiae was found in third-instar and adult C. sinensis , but was virtually restricted to third-instar C. destructor . Parasitoid phenology varied according to the instar and species of the host. Two fungal pathogens, Verticillium lecanii (Zimmermann) Viegas and Fusarium spp., were identified from both C. destructor and C. sinensis . Disease was a greater mortality factor than parasitism in C. destructor , whereas the opposite applied to those C. sinensis for which the cause of death could be identified. Disease levels were underestimated, particularly in C. destructor. Mortality from parasitism and disease did not act in a density-dependent manner.     

Allozyme relationships among ten species of Rhodniini, showing paraphyly of Rhodnius including Psammolestes

Genetic relationships among 10 species of bugs belonging to the tribe Rhodniini (Hemiptera: Reduviidae), including some important vectors of Chagas disease, were inferred from allozyme analysis of 12 enzyme loci (out of 21 enzyme systems examined), using agarose gel electrophoresis. These species formed two clusters: one comprising Rhodnius brethesi, R. ecuadoriensis, R. pallescens and R. pictipes; the other with Psammolestes tertius, Rhodnius domesticus and the Rhodnius prolixus group comprising R. nasutus, R. neglectus, R. prolixus and R. robustus. The resulting tree was [((R. ecuadoriensis, R. pallescens) R. brethesi) R. pictipes], [R. domesticus (P. tertius [(R. nasutus, R. neglectus) (R. prolixus, R. robustus)])]. Rhodnius nasutus and R. neglectus differed by only one locus, whereas no diagnostic loci were detected between R. prolixus and R. robustus (22 loci were analysed for these four species), despite considerable DNA sequence divergence between species in each of these pairs. Allozymes of the R. prolixus group showed greater similarity with Psammolestes tertius than with other Rhodnius spp., indicating that Rhodnius is paraphyletic and might include Psammolestes.     

Description d'une nouvelle espèce et analyse morpho-fonctionnelle du genre Doryaspis White (Heterostraci) du Dévonien du Spitsberg

Doryaspis groenhorgensis nov. sp. is a new pteraspidiform from the lower devonian of Spitsbergen. The genus Doryaspis is now considered as the most abundant pteraspidiform of the Wood Bay formation, with five described species. Moreover, the pteraspidiform diversity of this formation has been under rated all along the XXth century. A morpho-functional analysis of the Doryaspis generic characters (e.g. flat dorsal shield, ventral pseudorostrum, long cornual plates) allows to consider two possible mode of life. However, none of the pelagic or benthic mode of life is better supported than the other. The same analysis introduce some interpretative hypothesis on histology and moving of the Pteraspidiformes. The Pteraspidiformes diversity of Spitsbergen is important for further Devonian circum-arctic comparisons (e.g. siberian platform).     

Seasonal and Habitat Variability in the Fungal Pathogens, Neozygites cf. floridana and Hirsutella thompsonii, Associated with Cassava Mites in Benin, West Africa

A survey of the pathogenic fungi associated with mites on cassava in Benin, West Africa, revealed both geographical and seasonal variation in the presence of Neozygites cf. floridana (Weiser and Muma) and Hirsutella thompsonii Fisher on Mononychellus tanajoa (Bondar) and Oligonychus gossypii (Zacher). Few dead and infected mites were found during the dry season, regardless of vegetation zone. In three of 30 surveyed sites, N. floridana was found infecting 1% of the dead M. tanajoa and 2% of the dead O. gossypii, while H. thompsonii was observed infecting 20% of the dead M. tanajoa in a single site. The frequency of sites having infected mites during the wet season was 3.5 times greater than that seen during the dry season. N. floridana infected 10% of the dead M. tanajoa and 19% of the dead O. gossypii on young leaves. Mites infected with N. floridana were found either in the coastal Southern Forest Mosaic (SFM) or in the Northern Guinea Savanna vegetation zones. N. floridana was rare in the low mite densities associated with mature leaves. H. thompsonii was found on 19% and 29% of the dead M. tanajoa on young and mature leaves respectively. All M. tanajoa infected with H. thompsonii on young leaves and mature leaves (75%) were found in the SFM. A single M. tanajoa was the only infected mite found in the Southern Guinea Savanna. Relatively few O. gossypii were infected with H. thompsonii. N. floridana and H. thompsonii were found together in three sites, but never on the same host. Phytoseiids were never found infected with either pathogen. In a regression analysis, the number of dead mites was significantly estimated from the total number of mites for both species, regardless of leaf age. The numbers of dead M. tanajoa on mature leaves were also estimated from the proportion infected with H. thompsonii. The numbers of infected mites on young leaves were estimated from their association with the SFM for M. tanajoa infected with H. thompsonii, and from total mites for O. gossypii infected with N. floridana. On mature leaves, infected mite numbers were estimated from the numbers of dead M. tanajoa infected with H. thompsonii. The merit of introducing more virulent or better adapted isolates of N. floridana to control M. tanajoa in Africa is discussed.     

Revision of the Agathidinae (Hymenoptera, Braconidae) of Vietnam, with the description of forty-two new species and three new genera

The species of seventeen genera of Agathidinae (Braconidae) from Vietnam are revised: Agathis Latreille, 1804, Bassus Fabricius, 1804; Biroia Szépligeti, 1900; Braunsia Kriechbaumer, 1894; Camptothlipsis Enderlein, 1920; Coccygidium de Saussure, 1892; Coronagathis gen. n. (type species: Coronagathis cornifera sp. n.); Cremnops Foerster, 1862; Disophrys Foerster, 1862; Earinus Wesmael, 1837; Euagathis Szépligeti, 1900; Gyragathis gen. n. (type species: Gyragathis quyi sp. n.), Gyrochus Enderlein, 1920; Lytopylus Foerster, 1862; Therophilus Wesmael, 1837; Troticus Brullé, 1846, and Zelodia gen. n. (type species: Zelomorpha varipes van Achterberg & Maetô, 1990). Keys to the Vietnamese species are given.Sixty-five species are recognised, of which twelve species are newly recorded for Vietnam: Bassus albifasciatus (Watanabe, 1934), Coccygidium angostura (Bhat & Gupta, 1977), Cremnops atricornis (Smith, 1874), stat. n., Disophrys erythrocephala Cameron, 1900, Gyrochus yunnanensis Wang, 1984, Lytopylus romani (Shestakov, 1940), comb. n., Therophilus festivus (Muesebeck, 1953), comb. n., Therophilus javanus (Bhat & Gupta, 1977), comb. n., Therophilus lienhuachihensis (Chou & Sharkey, 1989), comb. n., Therophilus marshi (Bhat & Gupta, 1977), comb. n., Zelodia absoluta (Chen & Yang, 1998), comb. n. and Zelodia longidorsata (Bhat & Gupta, 1977), comb. n.Forty-two species are new to science: Agathis citrinisoma sp. n., Bassus albobasalis sp. n., Bassus albozonatus sp. n., Biroia soror sp. n., Braunsia bicolorata sp. n., Braunsia devriesi sp. n., Braunsia maculifera sp. n., Braunsia nigrapiculata sp. n., Braunsia pumatica sp. n., Camptothlipsis hanoiensis sp. n., Coronagathis cornifera sp. n., Earinus aurantius sp. n., Earinus brevistigmus sp. n., Euagathis flavosoma sp. n., Disophrys maculifera sp. n., Disophrys quymanhi sp. n., Disophrys rhinoides sp. n., Gyragathis quyi sp. n., Therophilus annuliferus sp. n., Therophilus cattienensis sp. n., Therophilus contrastus sp. n., Therophilus crenulisulcatus sp. n., Therophilus depressiferus sp. n., Therophilus elongator sp. n., Therophilus levisoma sp. n., Therophilus marucae sp. n., Therophilus mellisoma sp. n., Therophilus nigrolineatus sp. n., Therophilus nuichuaensis sp. n., Therophilus parasper sp. n., Therophilus planifrons sp. n., Therophilus punctiscutum sp. n., Therophilus robustus sp. n., Therophilus rugosiferus sp. n., Therophilus scutellatus sp. n., Troticus alloflavus sp. n., Troticus giganteus sp. n., Zelodia albobasalis sp. n., Zelodia anginota sp. n., Zelodia bicoloristigma sp. n., Zelodia brevifemoralis sp. n. and Zelodia flavistigma sp. n.The following new synonyms are proposed: Euagathis nigrithorax Bhat & Gupta, 1977, Euagathis variabilis Enderlein, 1920, Euagathis variabilis var. tibialis Enderlein, 1920, Euagathis variabilis var. melanopleura Enderlein, 1920 and Euagathis variabilis var. sucarandana Enderlein, 1920 with Euagathis abbotti (Ashmead, 1900); Euagathis jinshanensis Chen & Yang, 2006 and Euagathis sharkeyi Chen & Yang, 2006, with Euagathis forticarinata (Cameron, 1899). The genus Amputostypos Sharkey, 2009, is synonymised with Coccygidium de Saussure, 1892, syn. n.The following new combinations are given: Bassus subrasa (Enderlein, 1920), comb. n., Gyragathis angulosa (Bhat & Gupta, 1977), comb. n., Lytopylus romani (Shestakov, 1940), comb. n., Therophilus annulus (Chou & Sharkey, 1989), comb. n., Therophilus asper (Chou & Sharkey, 1989), comb. n., Therophilus cingulipes (Nees, 1812), comb. n., Therophilus daanyuanensis (Chen & Yang, 2006), comb. n., Therophilus fujianicus (Chen & Yang, 2006), comb. n., Therophilus javanus (Bhat & Gupta, 1977), comb. n., Therophilus lanyuensis (Chou & Sharkey, 1989), comb. n., Therophilus luzonicus (Bhat & Gupta, 1977), comb. n., Therophilus muesebecki (Bhat & Gupta, 1977), comb. n., Therophilus rudimentarius (Enderlein, 1920), comb. n., Therophilus similis (Bhat & Gupta, 1977), comb. n., Therophilus sungkangensis (Chou & Sharkey, 1989), comb. n., Therophilus tanycoleosus (Chen & Yang, 2006), comb. n., Therophilus tonghuaensis (Chen & Yang, 2006), comb. n., Therophilus tongmuensis (Chen & Yang, 2006), comb. n., Therophilus transcasperatus (Chen & Yang, 2006), comb. n., Troticus latiabdominalis (Bhat, 1978),comb. n., Zelodia absoluta (Chen & Yang, 1998), comb. n., Zelodia achterbergi (Chen & Yang, 2006), comb. n., Zelodia albopilosella (Cameron, 1908), comb. n., Zelodia chromoptera (Roman, 1913), comb. n., Zelodia nihonensis (Sharkey, 1996), comb. n., Zelodia cordata (Bhat & Gupta, 1977), comb. n., Zelodia diluta (Turner, 1918), comb. n., Zelodia dravida (Bhat & Gupta, 1977), comb. n., Zelodia exornata (Turner, 1918), comb. n., Zelodia longidorsata (Bhat & Gupta, 1977), comb. n., Zelodia longiptera (Yang & Chen, 2006), comb. n., Zelodia maculipes (Cameron, 1911), comb. n., Zelodia nigra (Bhat & Gupta, 1977), comb. n., Zelodia philippinensis (Bhat & Gupta, 1977), comb. n., Zelodia reticulosa (Yang & Chen, 2006), comb. n., Zelodia quadrifossulata (Enderlein, 1920), comb. n., Zelodia ruida (Sharkey, 1996), comb. n., Zelodia similis (Bhat & Gupta, 1977), comb. n., Zelodia penetrans (Smith, 1860), comb. n. and Zelodia varipes (van Achterberg & Maetô, 1990), comb. n.